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VARIANT - TERM ANNOTATION REPORT

1 Annotations Found.

An association has been curated linking CV32660 and autosomal recessive limb-girdle muscular dystrophy 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
  • 169 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy  (DOID:0110274)
  • 1 papers in RGD have been used to annotate CV32660
  • Curation Notes: ClinVar Annotator: match by term: Limb-Girdle Muscular Dystrophy, Recessive
  • Original References(s): PMID:10330340 PMID:10679950 PMID:14578192 PMID:14981715 PMID:15221789 PMID:15351423 PMID:15689361 PMID:15725583 PMID:16100770 PMID:16141003 PMID:16372320 PMID:16411092 PMID:16650086 PMID:17157502 PMID:17318636 PMID:17702496 PMID:20635405 PMID:21204801 PMID:21984748 PMID:25135358 PMID:25741868 PMID:26404900 PMID:26467025 PMID:26484845 PMID:27142102 PMID:28492532 PMID:28914264 PMID:30028523 PMID:30919934 PMID:31263448 PMID:31517061 PMID:31788660 PMID:7720071 PMID:9266733


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