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GENE - TERM ANNOTATION REPORT

115 Annotations Found.

An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9832443 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: CONGENITAL MYOPATHY 7B, MYOSIN STORAGE, AUTOSOMAL RECESSIVE
  • Original References(s): PMID:22958901 PMID:25741868 PMID:28492532 PMID:30403391 PMID:34598319


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10448659 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: CONGENITAL MYOPATHY 7B, MYOSIN STORAGE, AUTOSOMAL RECESSIVE
  • Original References(s): PMID:19412328 PMID:24093860 PMID:25741868 PMID:27247418 PMID:28255936 PMID:28492532 PMID:30297972 PMID:31019283 PMID:34542152


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8564083 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:12881443 PMID:15483641 PMID:18403758 PMID:21511876 PMID:23197161 PMID:23785128 PMID:24033266 PMID:24498601 PMID:24510615 PMID:25741868 PMID:25892673 PMID:27247418 PMID:27532257 PMID:28492532 PMID:28790153 PMID:30297972 PMID:31130376 PMID:32710294 PMID:34691145


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8564067 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:10521296 PMID:10882745 PMID:12975413 PMID:15010274 PMID:15856146 PMID:1638703 PMID:17612745 PMID:18029407 PMID:1975517 PMID:21310275 PMID:23751935 PMID:24033266 PMID:25741868 PMID:27532257 PMID:28492532 PMID:28790153 PMID:29300372 PMID:30924982 PMID:7662452 PMID:7848420 PMID:8186698 PMID:8254035 PMID:8268932


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9833163 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:31130376


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8605792 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:24033266 PMID:25741868 PMID:27247418 PMID:28492532 PMID:28771489 PMID:34542152


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9691955 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: CONGENITAL MYOPATHY 7B, MYOSIN STORAGE, AUTOSOMAL RECESSIVE
  • Original References(s): PMID:25611685 PMID:25741868 PMID:27532257 PMID:28492532 PMID:30696458


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8569690 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:15483641 PMID:21310275 PMID:23054336 PMID:23197161 PMID:23299917 PMID:23403236 PMID:23861362 PMID:24033266 PMID:24047955 PMID:24510615 PMID:25637381 PMID:25741868 PMID:26573135 PMID:27153395 PMID:27247418 PMID:28492532 PMID:29300372


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8605902 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:19412328 PMID:24033266 PMID:25741868 PMID:28492532 PMID:29300372 PMID:30847666


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8605701 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:10328076 PMID:10725281 PMID:10750581 PMID:11133230 PMID:11498078 PMID:11723028 PMID:12081993 PMID:12707239 PMID:12820698 PMID:15358028 PMID:15563892 PMID:15858117 PMID:16199542 PMID:17125710 PMID:17560888 PMID:18374998 PMID:18383048 PMID:18403758 PMID:18533079 PMID:19150014 PMID:20800588 PMID:21310275 PMID:21959974 PMID:22112859 PMID:22857948 PMID:23233322 PMID:23283745 PMID:23290139 PMID:23299917 PMID:23396983 PMID:23690394 PMID:24033266 PMID:24093860 PMID:24793961 PMID:25132132 PMID:25637381 PMID:25741868 PMID:26914223 PMID:26936621 PMID:27247418 PMID:27532257 PMID:28492532 PMID:29121657 PMID:29300372 PMID:29907873 PMID:30217213 PMID:31006259 PMID:31447099 PMID:31513939 PMID:31737537 PMID:31931472 PMID:32284968 PMID:7731997 PMID:9835779


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9833199 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: CONGENITAL MYOPATHY 7B, MYOSIN STORAGE, AUTOSOMAL RECESSIVE
  • Original References(s): PMID:25741868 PMID:28492532 PMID:34490048


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26906967 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:28492532 PMID:31130376


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8605771 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:15769782 PMID:15858117 PMID:24033266 PMID:25741868 PMID:28492532 PMID:29300372


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9833190 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: CONGENITAL MYOPATHY 7B, MYOSIN STORAGE, AUTOSOMAL RECESSIVE
  • Original References(s): PMID:25741868 PMID:27247418 PMID:28492532 PMID:32228044


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8564069 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:10882745 PMID:10957787 PMID:11904418 PMID:12084606 PMID:12707239 PMID:12974739 PMID:15000344 PMID:15858117 PMID:16504640 PMID:18414213 PMID:19645038 PMID:19651039 PMID:19659763 PMID:20378854 PMID:21310275 PMID:21769673 PMID:21896538 PMID:22429680 PMID:23816408 PMID:24033266 PMID:24510615 PMID:24829265 PMID:24888384 PMID:25611685 PMID:25741868 PMID:26912705 PMID:27082122 PMID:27247418 PMID:27532257 PMID:28296734 PMID:28408708 PMID:28492532 PMID:29029073 PMID:29300372 PMID:29907873 PMID:30775854 PMID:32612965 PMID:7731997 PMID:7874131 PMID:8282798 PMID:9001794 PMID:9154300 PMID:9544842 PMID:9822100 PMID:9829907


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10046372 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:23861362 PMID:25741868 PMID:28492532


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8564059 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:11968089 PMID:18761664 PMID:24793961 PMID:25741868 PMID:27532257 PMID:28492532 PMID:32894683 PMID:9544842


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8564052 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: CONGENITAL MYOPATHY 7B, MYOSIN STORAGE, AUTOSOMAL RECESSIVE
  • Original References(s): PMID:10086390 PMID:10606622 PMID:10725281 PMID:10764406 PMID:10874840 PMID:10882745 PMID:11227787 PMID:12084606 PMID:12601548 PMID:12707239 PMID:12820698 PMID:12975413 PMID:13732753 PMID:1423936 PMID:15358028 PMID:1552912 PMID:1634614 PMID:1638703 PMID:17351073 PMID:17987111 PMID:18403758 PMID:18565996 PMID:1975517 PMID:19808356 PMID:20031618 PMID:20800588 PMID:21239280 PMID:22213221 PMID:2249844 PMID:22735528 PMID:23054336 PMID:23580644 PMID:23751935 PMID:24033266 PMID:24268868 PMID:24793961 PMID:24928957 PMID:25611685 PMID:25741868 PMID:27247418 PMID:27532257 PMID:28492532 PMID:29300372 PMID:7788887 PMID:7789380 PMID:7883988 PMID:7994801 PMID:8281650 PMID:8514894 PMID:8614836 PMID:8898372 PMID:9105042 PMID:9140839 PMID:9172070 PMID:9541509 PMID:9826622


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8564053 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:10065021 PMID:11133230 PMID:11968089 PMID:12707239 PMID:12975413 PMID:1552912 PMID:18414213 PMID:1944483 PMID:22112859 PMID:23054336 PMID:23233322 PMID:23283745 PMID:23396983 PMID:23549607 PMID:24033266 PMID:24093860 PMID:24298987 PMID:24691700 PMID:25351510 PMID:25611685 PMID:25741868 PMID:25937619 PMID:26914223 PMID:27247418 PMID:27532257 PMID:27841901 PMID:28481356 PMID:28492532 PMID:29212898 PMID:29300372 PMID:7662452 PMID:7731997 PMID:9105042 PMID:9140839 PMID:9826622


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8564086 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:17372140 PMID:19336582 PMID:22918376 PMID:24033266 PMID:25741868 PMID:27532257 PMID:28125727 PMID:28492532 PMID:28973424


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8564056 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:11133230 PMID:11377367 PMID:11424919 PMID:12566107 PMID:12707239 PMID:1552912 PMID:15858117 PMID:16199542 PMID:17383184 PMID:18020371 PMID:18411228 PMID:20624503 PMID:20819418 PMID:21769673 PMID:24033266 PMID:24111713 PMID:24829265 PMID:24835277 PMID:25558701 PMID:25741868 PMID:27247418 PMID:27483260 PMID:28492532 PMID:29300372 PMID:30775854 PMID:7789380 PMID:8281650 PMID:8335820 PMID:8788376 PMID:8981935 PMID:9058851 PMID:9172070 PMID:9271024 PMID:9826622


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9691931 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:16858239 PMID:18533079 PMID:24033266 PMID:25741868 PMID:27247418 PMID:27532257 PMID:28492532


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8564057 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:10024460 PMID:12818575 PMID:12974739 PMID:1430197 PMID:15358028 PMID:1552912 PMID:15563892 PMID:16630449 PMID:18403758 PMID:18409188 PMID:22429680 PMID:22455086 PMID:23711808 PMID:24510615 PMID:25351510 PMID:25741868 PMID:27247418 PMID:27532257 PMID:28408708 PMID:28492532 PMID:29300372 PMID:31737537 PMID:34540771 PMID:7731997


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11352197 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:22429680 PMID:25741868 PMID:27532257 PMID:28492532 PMID:29540472


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8605855 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28152038 PMID:28492532 PMID:29300372 PMID:30471092 PMID:30588760 PMID:33500567 PMID:34542152 PMID:36129056


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9689064 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:22958901 PMID:24033266 PMID:24111713 PMID:24793961 PMID:25611685 PMID:25741868 PMID:26468400 PMID:27247418 PMID:27532257 PMID:27600940 PMID:28492532 PMID:28750076 PMID:28790153 PMID:28807990 PMID:31513939 PMID:31931689 PMID:32894683 PMID:33495597 PMID:34426522 PMID:34542152 PMID:35653365


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9688915 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:12707239 PMID:23861362 PMID:24033266 PMID:24793961 PMID:25467552 PMID:25741868 PMID:25961035 PMID:26627873 PMID:26969127 PMID:27247418 PMID:27532257 PMID:28492532 PMID:29300372 PMID:30297972 PMID:31918855 PMID:32894683 PMID:33673806 PMID:34542152


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151349186 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: CONGENITAL MYOPATHY 7B, MYOSIN STORAGE, AUTOSOMAL RECESSIVE
  • Original References(s): PMID:25741868 PMID:27247418 PMID:27532257 PMID:28492532


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9833202 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28138913 PMID:28492532


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151785100 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:25741868 PMID:28492532 PMID:29192238


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9833167 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:22918376 PMID:25447171 PMID:25741868 PMID:26718681 PMID:27247418 PMID:28492532 PMID:29192238 PMID:31156706


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9687256 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:19293840 PMID:21424860 PMID:21839045 PMID:22337857 PMID:23299917 PMID:23861362 PMID:25637381 PMID:25741868 PMID:28492532


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8605863 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:15556047 PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8605787 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:24033266 PMID:24503780 PMID:25741868 PMID:27247418 PMID:27532257 PMID:28492532


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14978119 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:25741868 PMID:28492532 PMID:32659924


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9833249 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:25351510 PMID:25741868 PMID:27532257 PMID:28492532 PMID:30984009


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8605932 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:15563892 PMID:16115294 PMID:16137545 PMID:16253604 PMID:17476457 PMID:18383048 PMID:19149795 PMID:19645038 PMID:20975235 PMID:22763267 PMID:23299917 PMID:23403236 PMID:23711808 PMID:23861362 PMID:24033266 PMID:25741868 PMID:26458567 PMID:26467025 PMID:27082122 PMID:27707468 PMID:28492532 PMID:29300372 PMID:8533830


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12884919 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:20530761 PMID:25741868 PMID:27532257 PMID:28492532 PMID:32880476


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:34894358 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: CONGENITAL MYOPATHY 7B, MYOSIN STORAGE, AUTOSOMAL RECESSIVE
  • Original References(s): PMID:16199547 PMID:25741868 PMID:28492532 PMID:29447731 PMID:29517769 PMID:30847666 PMID:33500567


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9833295 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:21750094 PMID:24111713 PMID:25741868 PMID:28492532 PMID:28807990 PMID:28971120 PMID:30188508


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8605832 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:11433818 PMID:12820698 PMID:12974739 PMID:15358028 PMID:15563892 PMID:18383048 PMID:20075948 PMID:21239446 PMID:21252143 PMID:21511876 PMID:22429680 PMID:22455086 PMID:22765922 PMID:23283745 PMID:24033266 PMID:24093860 PMID:24510615 PMID:25342278 PMID:25741868 PMID:26656175 PMID:26914223 PMID:27054166 PMID:27247418 PMID:27532257 PMID:28408708 PMID:28492532 PMID:29300372 PMID:33487615 PMID:33673806 PMID:8533830


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8605770 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: CONGENITAL MYOPATHY 7B, MYOSIN STORAGE, AUTOSOMAL RECESSIVE
  • Original References(s): PMID:15358028 PMID:24033266 PMID:25741868 PMID:28492532 PMID:29300372


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8605814 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:24033266 PMID:24503780 PMID:25741868 PMID:28492532 PMID:29300372


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8605818 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: CONGENITAL MYOPATHY 7B, MYOSIN STORAGE, AUTOSOMAL RECESSIVE
  • Original References(s): PMID:12707239 PMID:15358028 PMID:16352453 PMID:16858239 PMID:18409188 PMID:18533079 PMID:20624503 PMID:20800588 PMID:21239446 PMID:23674513 PMID:24033266 PMID:24111713 PMID:24510615 PMID:25031304 PMID:25741868 PMID:26743238 PMID:27247418 PMID:27532257 PMID:27688314 PMID:28202948 PMID:28492532 PMID:28687478 PMID:28971120 PMID:29101517 PMID:29169752 PMID:29300372 PMID:29343710 PMID:32344918


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8605827 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:15556047 PMID:20817590 PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8564063 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:11196015 PMID:12707239 PMID:15358028 PMID:15563892 PMID:15856146 PMID:19808356 PMID:20031618 PMID:20800588 PMID:21216834 PMID:22555271 PMID:24033266 PMID:24093860 PMID:24111713 PMID:24704860 PMID:24865491 PMID:25741868 PMID:25935763 PMID:27532257 PMID:28246639 PMID:28492532 PMID:29101517 PMID:29300372 PMID:7731997 PMID:7883988 PMID:8483915 PMID:8533830 PMID:9140824


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9833140 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:22958901 PMID:24111713 PMID:25741868 PMID:28492532 PMID:28798025 PMID:34426522 PMID:34542152


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9691936 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:15358028 PMID:16938236 PMID:19149795 PMID:20975235 PMID:22958901 PMID:24033266 PMID:24093860 PMID:24111713 PMID:24793961 PMID:25086479 PMID:25611685 PMID:25741868 PMID:25937619 PMID:26187847 PMID:27247418 PMID:27532257 PMID:28492532 PMID:28498465 PMID:28971120 PMID:31513939 PMID:31589614 PMID:32894683 PMID:33495597 PMID:34542152 PMID:35653365


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8605710 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: CONGENITAL MYOPATHY 7B, MYOSIN STORAGE, AUTOSOMAL RECESSIVE
  • Original References(s): PMID:24033266 PMID:25741868 PMID:26467025 PMID:27841901 PMID:28492532 PMID:29300372


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8605690 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: CONGENITAL MYOPATHY 7B, MYOSIN STORAGE, AUTOSOMAL RECESSIVE
  • Original References(s): PMID:15358028 PMID:24033266 PMID:24758099 PMID:25741868 PMID:26467025 PMID:28492532 PMID:29300372


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9833184 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:14659406 PMID:17372140 PMID:21310275 PMID:25666907 PMID:25741868 PMID:28492532 PMID:29170849 PMID:31130376


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8564087 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:17548557 PMID:21426742 PMID:21811976 PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8605767 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:10900182 PMID:15322983 PMID:16754800 PMID:17372140 PMID:17947214 PMID:19808347 PMID:19864899 PMID:20031602 PMID:20624503 PMID:20733148 PMID:20800588 PMID:2136805 PMID:21499742 PMID:21511876 PMID:22763267 PMID:22918376 PMID:22958901 PMID:23281406 PMID:23299917 PMID:23349452 PMID:23396983 PMID:23426552 PMID:23707328 PMID:23861362 PMID:24033266 PMID:24055113 PMID:24111713 PMID:24119082 PMID:24503780 PMID:25125180 PMID:25163546 PMID:25351510 PMID:25524337 PMID:25666907 PMID:25741868 PMID:26332594 PMID:26743238 PMID:28193612 PMID:28265379 PMID:28416588 PMID:28492532 PMID:28807990 PMID:28971120 PMID:29300372 PMID:29915098 PMID:30775854 PMID:31006259 PMID:3203908 PMID:7883988 PMID:7909436 PMID:8614836 PMID:8981935 PMID:9884344


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9691921 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: CONGENITAL MYOPATHY 7B, MYOSIN STORAGE, AUTOSOMAL RECESSIVE
  • Original References(s): PMID:20818890 PMID:24033266 PMID:25611685 PMID:25741868 PMID:26914223 PMID:27224906 PMID:27247418 PMID:27532257 PMID:28492532 PMID:28606303 PMID:33495597 PMID:34542152


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10448833 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:24111713 PMID:25741868 PMID:28356264 PMID:28408708 PMID:28492532 PMID:28790153 PMID:28971120 PMID:30327538


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11551341 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:22958901 PMID:25741868 PMID:28492532


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9833224 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:24691700 PMID:25741868 PMID:27066506 PMID:27532257 PMID:28492532 PMID:28771489


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13528660 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: CONGENITAL MYOPATHY 7B, MYOSIN STORAGE, AUTOSOMAL RECESSIVE
  • Original References(s): PMID:25741868 PMID:28356264 PMID:28492532


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9833168 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: CONGENITAL MYOPATHY 7B, MYOSIN STORAGE, AUTOSOMAL RECESSIVE
  • Original References(s): PMID:20800588 PMID:24664454 PMID:25214167 PMID:25741868 PMID:27387980 PMID:28492532 PMID:33906374


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11612467 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:25741868 PMID:28492532 PMID:32880476


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11548379 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: CONGENITAL MYOPATHY 7B, MYOSIN STORAGE, AUTOSOMAL RECESSIVE
  • Original References(s): PMID:10563488 PMID:12974739 PMID:20819418 PMID:22811549 PMID:23197161 PMID:24111713 PMID:25351510 PMID:25741868 PMID:27532257 PMID:28492532 PMID:28566242 PMID:31638223 PMID:32481709 PMID:33495596 PMID:33495597 PMID:34542152 PMID:35653365


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14394401 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:25741868 PMID:27532257 PMID:28492532 PMID:34935411


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9833164 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:25741868 PMID:27247418 PMID:28492532 PMID:30166250


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8605926 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:17438619 PMID:20031618 PMID:21896538 PMID:24033266 PMID:25351510 PMID:25741868 PMID:26743238 PMID:26914223 PMID:27247418 PMID:27532257 PMID:27974200 PMID:28138913 PMID:28408708 PMID:28492532 PMID:28615295 PMID:31006259


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8605700 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:10750581 PMID:11133230 PMID:12707239 PMID:15358028 PMID:15563892 PMID:15858117 PMID:18383048 PMID:18533079 PMID:20350521 PMID:20800588 PMID:22112859 PMID:23233322 PMID:23283745 PMID:23290139 PMID:23674513 PMID:23690394 PMID:23785128 PMID:24033266 PMID:25524337 PMID:25714468 PMID:25741868 PMID:27082122 PMID:27532257 PMID:28492532 PMID:30775854 PMID:31333075 PMID:31568572 PMID:32344918 PMID:32894683 PMID:33673806 PMID:35626289


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred from experiment (EXP)
  •  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: CTD Direct Evidence: marker/mechanism


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8605890 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:17125710 PMID:23396983 PMID:24033266 PMID:24111713 PMID:25351510 PMID:25741868 PMID:27532257 PMID:28492532 PMID:28606303 PMID:28771489 PMID:28840316 PMID:29687901 PMID:29875424 PMID:32531501 PMID:34495297 PMID:34542152 PMID:35276540


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9833158 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: CONGENITAL MYOPATHY 7B, MYOSIN STORAGE, AUTOSOMAL RECESSIVE
  • Original References(s): PMID:15483641 PMID:22555271 PMID:23054336 PMID:23299917 PMID:24111713 PMID:25741868 PMID:27194543 PMID:28492532 PMID:30847666 PMID:33232181 PMID:34542152 PMID:35653365


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9689057 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: CONGENITAL MYOPATHY 7B, MYOSIN STORAGE, AUTOSOMAL RECESSIVE
  • Original References(s): PMID:22464770 PMID:24093860 PMID:25741868 PMID:27532257 PMID:28492532


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8605684 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:24033266 PMID:24503780 PMID:25741868 PMID:27532257 PMID:28492532


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8605838 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: CONGENITAL MYOPATHY 7B, MYOSIN STORAGE, AUTOSOMAL RECESSIVE
  • Original References(s): PMID:15358028 PMID:15757018 PMID:17125710 PMID:19150014 PMID:21127202 PMID:22765922 PMID:22958901 PMID:23074333 PMID:23299917 PMID:23794396 PMID:24033266 PMID:24093860 PMID:24714796 PMID:24793961 PMID:25342278 PMID:25637381 PMID:25741868 PMID:27247418 PMID:28356264 PMID:28492532 PMID:28912206 PMID:29300372 PMID:30847666 PMID:30871747 PMID:31006259 PMID:33297573


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8605928 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:16199547 PMID:18506004 PMID:21551322 PMID:24033266 PMID:25741868 PMID:27788187 PMID:28492532


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12902120 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:23233322 PMID:25741868 PMID:28492532


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9833296 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:21310275 PMID:25741868 PMID:28492532 PMID:32163302 PMID:33495597


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8605797 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: CONGENITAL MYOPATHY 7B, MYOSIN STORAGE, AUTOSOMAL RECESSIVE
  • Original References(s): PMID:24033266 PMID:25741868 PMID:27247418 PMID:27532257 PMID:28492532 PMID:34542152


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9833174 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: CONGENITAL MYOPATHY 7B, MYOSIN STORAGE, AUTOSOMAL RECESSIVE
  • Original References(s): PMID:25741868 PMID:26220970 PMID:28492532 PMID:29773157 PMID:31983221 PMID:33297573


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14732897 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:25741868 PMID:28492532 PMID:31983221


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8605680|RGD:8605808|RGD:8605816|RGD:8605822 (Homo sapiens) & RGD:8605680|RGD:8605808|RGD:8605816|RGD:8605822 (Homo sapiens) & RGD:8605680|RGD:8605808|RGD:8605816|RGD:8605822 (Homo sapiens) & RGD:8605680|RGD:8605808|RGD:8605816|RGD:8605822 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: CONGENITAL MYOPATHY 7B, MYOSIN STORAGE, AUTOSOMAL RECESSIVE | ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126736025|RGD:126763003|RGD:127282658|RGD:12843612|RGD:12885181|RGD:12888017|RGD:13211460|RGD:13525966|RGD:13817347|RGD:14721784|RGD:14975426|RGD:15162087|RGD:151743717|RGD:26901375|RGD:26906775|RGD:34896767|RGD:34897458|RGD:34899138|RGD:34900218|RGD:9833067|RGD:9833111|RGD:9833131|RGD:9833176|RGD:9833209|RGD:9833294 (Homo sapiens) & RGD:126736025|RGD:126763003|RGD:127282658|RGD:12843612|RGD:12885181|RGD:12888017|RGD:13211460|RGD:13525966|RGD:13817347|RGD:14721784|RGD:14975426|RGD:15162087|RGD:151743717|RGD:26901375|RGD:26906775|RGD:34896767|RGD:34897458|RGD:34899138|RGD:34900218|RGD:9833067|RGD:9833111|RGD:9833131|RGD:9833176|RGD:9833209|RGD:9833294 (Homo sapiens) & RGD:126736025|RGD:126763003|RGD:127282658|RGD:12843612|RGD:12885181|RGD:12888017|RGD:13211460|RGD:13525966|RGD:13817347|RGD:14721784|RGD:14975426|RGD:15162087|RGD:151743717|RGD:26901375|RGD:26906775|RGD:34896767|RGD:34897458|RGD:34899138|RGD:34900218|RGD:9833067|RGD:9833111|RGD:9833131|RGD:9833176|RGD:9833209|RGD:9833294 (Homo sapiens) & RGD:126736025|RGD:126763003|RGD:127282658|RGD:12843612|RGD:12885181|RGD:12888017|RGD:13211460|RGD:13525966|RGD:13817347|RGD:14721784|RGD:14975426|RGD:15162087|RGD:151743717|RGD:26901375|RGD:26906775|RGD:34896767|RGD:34897458|RGD:34899138|RGD:34900218|RGD:9833067|RGD:9833111|RGD:9833131|RGD:9833176|RGD:9833209|RGD:9833294 (Homo sapiens) & RGD:126736025|RGD:126763003|RGD:127282658|RGD:12843612|RGD:12885181|RGD:12888017|RGD:13211460|RGD:13525966|RGD:13817347|RGD:14721784|RGD:14975426|RGD:15162087|RGD:151743717|RGD:26901375|RGD:26906775|RGD:34896767|RGD:34897458|RGD:34899138|RGD:34900218|RGD:9833067|RGD:9833111|RGD:9833131|RGD:9833176|RGD:9833209|RGD:9833294 (Homo sapiens) & RGD:126736025|RGD:126763003|RGD:127282658|RGD:12843612|RGD:12885181|RGD:12888017|RGD:13211460|RGD:13525966|RGD:13817347|RGD:14721784|RGD:14975426|RGD:15162087|RGD:151743717|RGD:26901375|RGD:26906775|RGD:34896767|RGD:34897458|RGD:34899138|RGD:34900218|RGD:9833067|RGD:9833111|RGD:9833131|RGD:9833176|RGD:9833209|RGD:9833294 (Homo sapiens) & RGD:126736025|RGD:126763003|RGD:127282658|RGD:12843612|RGD:12885181|RGD:12888017|RGD:13211460|RGD:13525966|RGD:13817347|RGD:14721784|RGD:14975426|RGD:15162087|RGD:151743717|RGD:26901375|RGD:26906775|RGD:34896767|RGD:34897458|RGD:34899138|RGD:34900218|RGD:9833067|RGD:9833111|RGD:9833131|RGD:9833176|RGD:9833209|RGD:9833294 (Homo sapiens) & RGD:126736025|RGD:126763003|RGD:127282658|RGD:12843612|RGD:12885181|RGD:12888017|RGD:13211460|RGD:13525966|RGD:13817347|RGD:14721784|RGD:14975426|RGD:15162087|RGD:151743717|RGD:26901375|RGD:26906775|RGD:34896767|RGD:34897458|RGD:34899138|RGD:34900218|RGD:9833067|RGD:9833111|RGD:9833131|RGD:9833176|RGD:9833209|RGD:9833294 (Homo sapiens) & RGD:126736025|RGD:126763003|RGD:127282658|RGD:12843612|RGD:12885181|RGD:12888017|RGD:13211460|RGD:13525966|RGD:13817347|RGD:14721784|RGD:14975426|RGD:15162087|RGD:151743717|RGD:26901375|RGD:26906775|RGD:34896767|RGD:34897458|RGD:34899138|RGD:34900218|RGD:9833067|RGD:9833111|RGD:9833131|RGD:9833176|RGD:9833209|RGD:9833294 (Homo sapiens) & RGD:126736025|RGD:126763003|RGD:127282658|RGD:12843612|RGD:12885181|RGD:12888017|RGD:13211460|RGD:13525966|RGD:13817347|RGD:14721784|RGD:14975426|RGD:15162087|RGD:151743717|RGD:26901375|RGD:26906775|RGD:34896767|RGD:34897458|RGD:34899138|RGD:34900218|RGD:9833067|RGD:9833111|RGD:9833131|RGD:9833176|RGD:9833209|RGD:9833294 (Homo sapiens) & RGD:126736025|RGD:126763003|RGD:127282658|RGD:12843612|RGD:12885181|RGD:12888017|RGD:13211460|RGD:13525966|RGD:13817347|RGD:14721784|RGD:14975426|RGD:15162087|RGD:151743717|RGD:26901375|RGD:26906775|RGD:34896767|RGD:34897458|RGD:34899138|RGD:34900218|RGD:9833067|RGD:9833111|RGD:9833131|RGD:9833176|RGD:9833209|RGD:9833294 (Homo sapiens) & RGD:126736025|RGD:126763003|RGD:127282658|RGD:12843612|RGD:12885181|RGD:12888017|RGD:13211460|RGD:13525966|RGD:13817347|RGD:14721784|RGD:14975426|RGD:15162087|RGD:151743717|RGD:26901375|RGD:26906775|RGD:34896767|RGD:34897458|RGD:34899138|RGD:34900218|RGD:9833067|RGD:9833111|RGD:9833131|RGD:9833176|RGD:9833209|RGD:9833294 (Homo sapiens) & RGD:126736025|RGD:126763003|RGD:127282658|RGD:12843612|RGD:12885181|RGD:12888017|RGD:13211460|RGD:13525966|RGD:13817347|RGD:14721784|RGD:14975426|RGD:15162087|RGD:151743717|RGD:26901375|RGD:26906775|RGD:34896767|RGD:34897458|RGD:34899138|RGD:34900218|RGD:9833067|RGD:9833111|RGD:9833131|RGD:9833176|RGD:9833209|RGD:9833294 (Homo sapiens) & RGD:126736025|RGD:126763003|RGD:127282658|RGD:12843612|RGD:12885181|RGD:12888017|RGD:13211460|RGD:13525966|RGD:13817347|RGD:14721784|RGD:14975426|RGD:15162087|RGD:151743717|RGD:26901375|RGD:26906775|RGD:34896767|RGD:34897458|RGD:34899138|RGD:34900218|RGD:9833067|RGD:9833111|RGD:9833131|RGD:9833176|RGD:9833209|RGD:9833294 (Homo sapiens) & RGD:126736025|RGD:126763003|RGD:127282658|RGD:12843612|RGD:12885181|RGD:12888017|RGD:13211460|RGD:13525966|RGD:13817347|RGD:14721784|RGD:14975426|RGD:15162087|RGD:151743717|RGD:26901375|RGD:26906775|RGD:34896767|RGD:34897458|RGD:34899138|RGD:34900218|RGD:9833067|RGD:9833111|RGD:9833131|RGD:9833176|RGD:9833209|RGD:9833294 (Homo sapiens) & RGD:126736025|RGD:126763003|RGD:127282658|RGD:12843612|RGD:12885181|RGD:12888017|RGD:13211460|RGD:13525966|RGD:13817347|RGD:14721784|RGD:14975426|RGD:15162087|RGD:151743717|RGD:26901375|RGD:26906775|RGD:34896767|RGD:34897458|RGD:34899138|RGD:34900218|RGD:9833067|RGD:9833111|RGD:9833131|RGD:9833176|RGD:9833209|RGD:9833294 (Homo sapiens) & RGD:126736025|RGD:126763003|RGD:127282658|RGD:12843612|RGD:12885181|RGD:12888017|RGD:13211460|RGD:13525966|RGD:13817347|RGD:14721784|RGD:14975426|RGD:15162087|RGD:151743717|RGD:26901375|RGD:26906775|RGD:34896767|RGD:34897458|RGD:34899138|RGD:34900218|RGD:9833067|RGD:9833111|RGD:9833131|RGD:9833176|RGD:9833209|RGD:9833294 (Homo sapiens) & RGD:126736025|RGD:126763003|RGD:127282658|RGD:12843612|RGD:12885181|RGD:12888017|RGD:13211460|RGD:13525966|RGD:13817347|RGD:14721784|RGD:14975426|RGD:15162087|RGD:151743717|RGD:26901375|RGD:26906775|RGD:34896767|RGD:34897458|RGD:34899138|RGD:34900218|RGD:9833067|RGD:9833111|RGD:9833131|RGD:9833176|RGD:9833209|RGD:9833294 (Homo sapiens) & RGD:126736025|RGD:126763003|RGD:127282658|RGD:12843612|RGD:12885181|RGD:12888017|RGD:13211460|RGD:13525966|RGD:13817347|RGD:14721784|RGD:14975426|RGD:15162087|RGD:151743717|RGD:26901375|RGD:26906775|RGD:34896767|RGD:34897458|RGD:34899138|RGD:34900218|RGD:9833067|RGD:9833111|RGD:9833131|RGD:9833176|RGD:9833209|RGD:9833294 (Homo sapiens) & RGD:126736025|RGD:126763003|RGD:127282658|RGD:12843612|RGD:12885181|RGD:12888017|RGD:13211460|RGD:13525966|RGD:13817347|RGD:14721784|RGD:14975426|RGD:15162087|RGD:151743717|RGD:26901375|RGD:26906775|RGD:34896767|RGD:34897458|RGD:34899138|RGD:34900218|RGD:9833067|RGD:9833111|RGD:9833131|RGD:9833176|RGD:9833209|RGD:9833294 (Homo sapiens) & RGD:126736025|RGD:126763003|RGD:127282658|RGD:12843612|RGD:12885181|RGD:12888017|RGD:13211460|RGD:13525966|RGD:13817347|RGD:14721784|RGD:14975426|RGD:15162087|RGD:151743717|RGD:26901375|RGD:26906775|RGD:34896767|RGD:34897458|RGD:34899138|RGD:34900218|RGD:9833067|RGD:9833111|RGD:9833131|RGD:9833176|RGD:9833209|RGD:9833294 (Homo sapiens) & RGD:126736025|RGD:126763003|RGD:127282658|RGD:12843612|RGD:12885181|RGD:12888017|RGD:13211460|RGD:13525966|RGD:13817347|RGD:14721784|RGD:14975426|RGD:15162087|RGD:151743717|RGD:26901375|RGD:26906775|RGD:34896767|RGD:34897458|RGD:34899138|RGD:34900218|RGD:9833067|RGD:9833111|RGD:9833131|RGD:9833176|RGD:9833209|RGD:9833294 (Homo sapiens) & RGD:126736025|RGD:126763003|RGD:127282658|RGD:12843612|RGD:12885181|RGD:12888017|RGD:13211460|RGD:13525966|RGD:13817347|RGD:14721784|RGD:14975426|RGD:15162087|RGD:151743717|RGD:26901375|RGD:26906775|RGD:34896767|RGD:34897458|RGD:34899138|RGD:34900218|RGD:9833067|RGD:9833111|RGD:9833131|RGD:9833176|RGD:9833209|RGD:9833294 (Homo sapiens) & RGD:126736025|RGD:126763003|RGD:127282658|RGD:12843612|RGD:12885181|RGD:12888017|RGD:13211460|RGD:13525966|RGD:13817347|RGD:14721784|RGD:14975426|RGD:15162087|RGD:151743717|RGD:26901375|RGD:26906775|RGD:34896767|RGD:34897458|RGD:34899138|RGD:34900218|RGD:9833067|RGD:9833111|RGD:9833131|RGD:9833176|RGD:9833209|RGD:9833294 (Homo sapiens) & RGD:126736025|RGD:126763003|RGD:127282658|RGD:12843612|RGD:12885181|RGD:12888017|RGD:13211460|RGD:13525966|RGD:13817347|RGD:14721784|RGD:14975426|RGD:15162087|RGD:151743717|RGD:26901375|RGD:26906775|RGD:34896767|RGD:34897458|RGD:34899138|RGD:34900218|RGD:9833067|RGD:9833111|RGD:9833131|RGD:9833176|RGD:9833209|RGD:9833294 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: CONGENITAL MYOPATHY 7B, MYOSIN STORAGE, AUTOSOMAL RECESSIVE | ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9688419 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: CONGENITAL MYOPATHY 7B, MYOSIN STORAGE, AUTOSOMAL RECESSIVE
  • Original References(s): PMID:10862102 PMID:12974739 PMID:12975413 PMID:17192269 PMID:17703256 PMID:19149795 PMID:20075948 PMID:20298698 PMID:20975235 PMID:22112859 PMID:23299917 PMID:24033266 PMID:24621997 PMID:25132132 PMID:25637381 PMID:25741868 PMID:27247418 PMID:27532257 PMID:28492532 PMID:28771489 PMID:29300372 PMID:29907873 PMID:30022097 PMID:30206291 PMID:30217213 PMID:32492895 PMID:32931854 PMID:33407484 PMID:33495596 PMID:33495597 PMID:34949102 PMID:36005429 PMID:7796500 PMID:9172070


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8605813 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:24033266 PMID:25741868 PMID:27532257 PMID:28492532 PMID:29773157 PMID:31918855 PMID:31983221


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9833217 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: CONGENITAL MYOPATHY 7B, MYOSIN STORAGE, AUTOSOMAL RECESSIVE
  • Original References(s): PMID:12707239 PMID:23816408 PMID:24111713 PMID:24865491 PMID:25741868 PMID:27247418 PMID:27532257 PMID:27841901 PMID:28492532 PMID:36264615


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26907313 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:16199547 PMID:25741868 PMID:28492532 PMID:29343803 PMID:36923113


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8605727 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:10521296 PMID:11186938 PMID:11447480 PMID:15358028 PMID:16858239 PMID:17125710 PMID:18029407 PMID:19880069 PMID:20031618 PMID:21310275 PMID:22857948 PMID:22975586 PMID:23233322 PMID:23283745 PMID:23299917 PMID:24033266 PMID:24038877 PMID:24093860 PMID:24111713 PMID:24793961 PMID:25031304 PMID:25351510 PMID:25637381 PMID:25741868 PMID:26743238 PMID:26969327 PMID:27247418 PMID:27532257 PMID:27737317 PMID:27831900 PMID:27841901 PMID:28138913 PMID:28420666 PMID:28492532 PMID:28606303 PMID:28615295 PMID:28790153 PMID:30291343 PMID:30755392 PMID:31006259 PMID:31110529 PMID:31447099 PMID:31589614 PMID:32233023 PMID:33297573 PMID:33673806 PMID:7581410


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11040010 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: CONGENITAL MYOPATHY 7B, MYOSIN STORAGE, AUTOSOMAL RECESSIVE
  • Original References(s): PMID:25741868 PMID:28492532 PMID:30775854


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8605829 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:15358028 PMID:20624503 PMID:20800588 PMID:21817903 PMID:22958901 PMID:23140321 PMID:23283745 PMID:23299917 PMID:23403236 PMID:24033266 PMID:24055113 PMID:24111713 PMID:24664454 PMID:25132132 PMID:25637381 PMID:25741868 PMID:25961035 PMID:26914223 PMID:27247418 PMID:27532257 PMID:27841901 PMID:28492532 PMID:28640247 PMID:29300372 PMID:30297972 PMID:30696458 PMID:33190526 PMID:34542152 PMID:35544052 PMID:35653365


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8564060 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:12117842 PMID:12707239 PMID:1430197 PMID:14563299 PMID:16199542 PMID:18533079 PMID:20359594 PMID:20819418 PMID:21310275 PMID:21835320 PMID:23074333 PMID:24033266 PMID:24510615 PMID:25239116 PMID:25741868 PMID:25935763 PMID:27247418 PMID:27532257 PMID:27841901 PMID:28492532 PMID:29300372 PMID:29709087 PMID:29710196 PMID:29875424 PMID:31245010 PMID:32481709 PMID:32880476 PMID:33495596 PMID:33495597 PMID:33673806 PMID:34135346 PMID:35384713 PMID:35535697 PMID:35784482 PMID:36843271 PMID:7546620 PMID:7612980 PMID:7713108 PMID:7731997 PMID:7815466 PMID:8180512 PMID:8194835 PMID:8196066 PMID:8282798 PMID:8375803 PMID:8533830 PMID:8541871 PMID:9140839 PMID:9202846 PMID:9503187 PMID:9742053 PMID:9829907 PMID:9835779


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14689074 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:25741868 PMID:27247418 PMID:28492532 PMID:33241513 PMID:35993536


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8605748 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: CONGENITAL MYOPATHY 7B, MYOSIN STORAGE, AUTOSOMAL RECESSIVE
  • Original References(s): PMID:15358028 PMID:15519027 PMID:15858117 PMID:18761664 PMID:21511876 PMID:23396983 PMID:24033266 PMID:24510615 PMID:24793961 PMID:25351510 PMID:25741868 PMID:26914223 PMID:27532257 PMID:28408708 PMID:28492532 PMID:28615295 PMID:28790153 PMID:29300372 PMID:32228044 PMID:32894683 PMID:33495597 PMID:34556856 PMID:35026164


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8602987 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: CONGENITAL MYOPATHY 7B, MYOSIN STORAGE, AUTOSOMAL RECESSIVE
  • Original References(s): PMID:15483641 PMID:18403758 PMID:20298698 PMID:21511876 PMID:23054336 PMID:23074333 PMID:23197161 PMID:23785128 PMID:24033266 PMID:24498601 PMID:24510615 PMID:24714796 PMID:24835277 PMID:25351510 PMID:25741868 PMID:25892673 PMID:27247418 PMID:27532257 PMID:27688314 PMID:28193612 PMID:28241245 PMID:28492532 PMID:28771489 PMID:28794111 PMID:29300372 PMID:29661763 PMID:30022097 PMID:30297972 PMID:30531895 PMID:30847666 PMID:31308319 PMID:31447099 PMID:31737537 PMID:32894683 PMID:33495596 PMID:33495597 PMID:33673806 PMID:34352619 PMID:34542152 PMID:34830538 PMID:35026164 PMID:35176171 PMID:35626289 PMID:37488328 PMID:564455


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9688847 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:11861410 PMID:11861413 PMID:15136674 PMID:16918501 PMID:21239446 PMID:24033266 PMID:24510615 PMID:25741868 PMID:27247418 PMID:27532257 PMID:28492532 PMID:28518168 PMID:29121657 PMID:29300372 PMID:30297972 PMID:30731207 PMID:30847666 PMID:31199839 PMID:31493341 PMID:33495597 PMID:34136434 PMID:34137518 PMID:34542152


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8605944 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:19666645 PMID:23299917 PMID:24033266 PMID:24183960 PMID:25637381 PMID:25741868 PMID:27153395 PMID:27247418 PMID:27476098 PMID:27532257 PMID:28492532 PMID:29447731 PMID:29875424 PMID:30696458 PMID:31323898 PMID:31513939 PMID:32369506 PMID:32627857 PMID:33495597 PMID:34426522 PMID:37466024


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8605802 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:23283745 PMID:24033266 PMID:25741868 PMID:27532257 PMID:28492532 PMID:31104103


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8605873 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:19659763 PMID:21302287 PMID:24033266 PMID:25741868 PMID:27247418 PMID:27532257 PMID:28356264 PMID:28408708 PMID:28492532 PMID:28790153 PMID:32528171 PMID:33495596 PMID:33495597 PMID:33588347 PMID:34542152 PMID:36129056


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9687904 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:15322983 PMID:15556047 PMID:18660445 PMID:19412328 PMID:19854198 PMID:22155079 PMID:22337857 PMID:23153285 PMID:23403236 PMID:24033266 PMID:24047955 PMID:24119082 PMID:25741868 PMID:25961035 PMID:26383716 PMID:28492532 PMID:28750076 PMID:30122538 PMID:31317183 PMID:33500567 PMID:34542152 PMID:737223 PMID:901918


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8605876 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:24033266 PMID:25611685 PMID:25741868 PMID:27532257 PMID:28492532 PMID:31983222 PMID:33495597


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8605774 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:18533079 PMID:19659763 PMID:1976477 PMID:20215591 PMID:24033266 PMID:24793961 PMID:25611685 PMID:25741868 PMID:26914223 PMID:27000522 PMID:27247418 PMID:27532257 PMID:28492532 PMID:29764897 PMID:33495596 PMID:33495597 PMID:34503678 PMID:34542152 PMID:35732239


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13475432 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: CONGENITAL MYOPATHY 7B, MYOSIN STORAGE, AUTOSOMAL RECESSIVE
  • Original References(s): PMID:23403236 PMID:25741868 PMID:26467025 PMID:28492532 PMID:33815637


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9688843 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: CONGENITAL MYOPATHY 7B, MYOSIN STORAGE, AUTOSOMAL RECESSIVE
  • Original References(s): PMID:15856146 PMID:19666645 PMID:20646679 PMID:24033266 PMID:24111713 PMID:24835277 PMID:25611685 PMID:25741868 PMID:27247418 PMID:27532257 PMID:2840870 PMID:28408708 PMID:28492532 PMID:28606303 PMID:28615295 PMID:30275503 PMID:30847666 PMID:30868567 PMID:31447099 PMID:32894683 PMID:33673806 PMID:33764162 PMID:34542152


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8564090 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:12081993 PMID:15528230 PMID:16267253 PMID:18761664 PMID:21310275 PMID:23054336 PMID:24033266 PMID:24510615 PMID:24704860 PMID:25351510 PMID:25741868 PMID:26914223 PMID:27247418 PMID:27532257 PMID:28193612 PMID:28241245 PMID:28481356 PMID:28492532 PMID:28606303 PMID:29300372 PMID:33495597 PMID:35026164


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9688885 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:15358028 PMID:15563892 PMID:16858239 PMID:17180650 PMID:18533079 PMID:1976466 PMID:20173211 PMID:20359594 PMID:21835320 PMID:22763267 PMID:22958901 PMID:23674513 PMID:24033266 PMID:24093860 PMID:24793961 PMID:25078086 PMID:25351510 PMID:25524337 PMID:25741868 PMID:26332594 PMID:27247418 PMID:27532257 PMID:28492532 PMID:29121657 PMID:29300372 PMID:29710196 PMID:30297972 PMID:30588760 PMID:31112422 PMID:31447099 PMID:32380161 PMID:32894683 PMID:33382884 PMID:35653365 PMID:36203036


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8605811 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:24503780 PMID:25741868 PMID:27532257 PMID:28492532 PMID:30511546 PMID:35470680


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11351623|RGD:9833187 (Homo sapiens) & RGD:11351623|RGD:9833187 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: CONGENITAL MYOPATHY 7B, MYOSIN STORAGE, AUTOSOMAL RECESSIVE | ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:25741868 PMID:27532257 PMID:28492532


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9691120 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:18409188 PMID:20513729 PMID:24033266 PMID:25741868 PMID:27247418 PMID:28492532


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8605695|RGD:8605882 (Homo sapiens) & RGD:8605695|RGD:8605882 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:18414213 PMID:24033266 PMID:25741868 PMID:28492532 PMID:29300372


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8605669|RGD:8605783 (Homo sapiens) & RGD:8605669|RGD:8605783 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: CONGENITAL MYOPATHY 7B, MYOSIN STORAGE, AUTOSOMAL RECESSIVE | ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532 PMID:29300372


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8605666 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:21239446 PMID:21750094 PMID:24033266 PMID:25741868 PMID:26914223 PMID:27247418 PMID:27532257 PMID:27688314 PMID:28408708 PMID:28492532 PMID:28615295 PMID:28640247 PMID:28790153 PMID:29121657 PMID:30297972 PMID:31068177 PMID:31213605 PMID:32894683 PMID:35026164


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8605921 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:12707239 PMID:20439259 PMID:20975235 PMID:22429680 PMID:23074333 PMID:23816408 PMID:24033266 PMID:24111713 PMID:24865491 PMID:25741868 PMID:27247418 PMID:27532257 PMID:27841901 PMID:2790153 PMID:28492532 PMID:28790153 PMID:28986452 PMID:29970176 PMID:32894683 PMID:35653365


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13534225|RGD:9833153 (Homo sapiens) & RGD:13534225|RGD:9833153 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: CONGENITAL MYOPATHY 7B, MYOSIN STORAGE, AUTOSOMAL RECESSIVE | ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:17576681 PMID:25741868 PMID:28492532 PMID:9536098


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11345627|RGD:126759230|RGD:13609210|RGD:26904775|RGD:9833171 (Homo sapiens) & RGD:11345627|RGD:126759230|RGD:13609210|RGD:26904775|RGD:9833171 (Homo sapiens) & RGD:11345627|RGD:126759230|RGD:13609210|RGD:26904775|RGD:9833171 (Homo sapiens) & RGD:11345627|RGD:126759230|RGD:13609210|RGD:26904775|RGD:9833171 (Homo sapiens) & RGD:11345627|RGD:126759230|RGD:13609210|RGD:26904775|RGD:9833171 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: CONGENITAL MYOPATHY 7B, MYOSIN STORAGE, AUTOSOMAL RECESSIVE | ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:25741868 PMID:27247418 PMID:28492532


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:150507372|RGD:34900138|RGD:401875742|RGD:401941723 (Homo sapiens) & RGD:150507372|RGD:34900138|RGD:401875742|RGD:401941723 (Homo sapiens) & RGD:150507372|RGD:34900138|RGD:401875742|RGD:401941723 (Homo sapiens) & RGD:150507372|RGD:34900138|RGD:401875742|RGD:401941723 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: CONGENITAL MYOPATHY 7B, MYOSIN STORAGE, AUTOSOMAL RECESSIVE | ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:25741868


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12850242 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:12016059 PMID:16870472 PMID:17576681 PMID:25125180 PMID:25741868 PMID:26782017 PMID:27387980 PMID:28492532 PMID:30794915 PMID:33333461 PMID:9047366 PMID:9536098


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8605927 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:16267253 PMID:18506004 PMID:20350521 PMID:20965760 PMID:21551322 PMID:21799269 PMID:24033266 PMID:25132132 PMID:25741868 PMID:27247418 PMID:27532257 PMID:28492532 PMID:29121657 PMID:30297972 PMID:32815737 PMID:32830170 PMID:33705529


  • An association has been curated linking MYH7 and autosomal recessive hyaline body myopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9833109 (Homo sapiens)
  • 4 RGD objects have been annotated to autosomal recessive hyaline body myopathy  (DOID:0111268)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myosin storage, autosomal recessive
  • Original References(s): PMID:25741868 PMID:27483260 PMID:27600940 PMID:28492532 PMID:31589614


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