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GENE - TERM ANNOTATION REPORT

34 Annotations Found.

An association has been curated linking STON1-GTF2A1L and Hypergonadotropic hypogonadism 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:11547555 (Homo sapiens)
  • 68 RGD objects have been annotated to Hypergonadotropic hypogonadism  (HP:0000815)
  • 2 papers in RGD have been used to annotate STON1-GTF2A1L
  • Curation Notes: ClinVar Annotator: match by term: Hypergonadotropic hypogonadism
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


    • An association has been curated linking STON1-GTF2A1L and Hypergonadotropic hypogonadism 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:11548938 (Homo sapiens)
  • 68 RGD objects have been annotated to Hypergonadotropic hypogonadism  (HP:0000815)
  • 2 papers in RGD have been used to annotate STON1-GTF2A1L
  • Curation Notes: ClinVar Annotator: match by term: Hypergonadotropic hypogonadism
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


    • An association has been curated linking STON1-GTF2A1L and Hypergonadotropic hypogonadism 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:11543955 (Homo sapiens)
  • 68 RGD objects have been annotated to Hypergonadotropic hypogonadism  (HP:0000815)
  • 2 papers in RGD have been used to annotate STON1-GTF2A1L
  • Curation Notes: ClinVar Annotator: match by term: Hypergonadotropic hypogonadism
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


    • An association has been curated linking STON1-GTF2A1L and Hypergonadotropic hypogonadism 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:8691852 (Homo sapiens)
  • 68 RGD objects have been annotated to Hypergonadotropic hypogonadism  (HP:0000815)
  • 2 papers in RGD have been used to annotate STON1-GTF2A1L
  • Curation Notes: ClinVar Annotator: match by term: Hypergonadotropic hypogonadism
  • Original References(s): PMID:28492532


    • An association has been curated linking STON1-GTF2A1L and Hypergonadotropic hypogonadism 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:11589976 (Homo sapiens)
  • 68 RGD objects have been annotated to Hypergonadotropic hypogonadism  (HP:0000815)
  • 2 papers in RGD have been used to annotate STON1-GTF2A1L
  • Curation Notes: ClinVar Annotator: match by term: Primary hypogonadism


    • An association has been curated linking STON1-GTF2A1L and Hypergonadotropic hypogonadism 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:11584981 (Homo sapiens)
  • 68 RGD objects have been annotated to Hypergonadotropic hypogonadism  (HP:0000815)
  • 2 papers in RGD have been used to annotate STON1-GTF2A1L
  • Curation Notes: ClinVar Annotator: match by term: Primary hypogonadism


    • An association has been curated linking STON1-GTF2A1L and Hypergonadotropic hypogonadism 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:11653177 (Homo sapiens)
  • 68 RGD objects have been annotated to Hypergonadotropic hypogonadism  (HP:0000815)
  • 2 papers in RGD have been used to annotate STON1-GTF2A1L
  • Curation Notes: ClinVar Annotator: match by term: Primary hypogonadism


    • An association has been curated linking STON1-GTF2A1L and Hypergonadotropic hypogonadism 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:11586667 (Homo sapiens)
  • 68 RGD objects have been annotated to Hypergonadotropic hypogonadism  (HP:0000815)
  • 2 papers in RGD have been used to annotate STON1-GTF2A1L
  • Curation Notes: ClinVar Annotator: match by term: Primary hypogonadism


    • An association has been curated linking STON1-GTF2A1L and Hypergonadotropic hypogonadism 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:11588947 (Homo sapiens)
  • 68 RGD objects have been annotated to Hypergonadotropic hypogonadism  (HP:0000815)
  • 2 papers in RGD have been used to annotate STON1-GTF2A1L
  • Curation Notes: ClinVar Annotator: match by term: Primary hypogonadism
  • Original References(s): PMID:28492532


    • An association has been curated linking STON1-GTF2A1L and Hypergonadotropic hypogonadism 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:8602917 (Homo sapiens)
  • 68 RGD objects have been annotated to Hypergonadotropic hypogonadism  (HP:0000815)
  • 2 papers in RGD have been used to annotate STON1-GTF2A1L
  • Curation Notes: ClinVar Annotator: match by term: Primary hypogonadism
  • Original References(s): PMID:28492532


    • An association has been curated linking STON1-GTF2A1L and Hypergonadotropic hypogonadism 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:11585614 (Homo sapiens)
  • 68 RGD objects have been annotated to Hypergonadotropic hypogonadism  (HP:0000815)
  • 2 papers in RGD have been used to annotate STON1-GTF2A1L
  • Curation Notes: ClinVar Annotator: match by term: Primary hypogonadism


    • An association has been curated linking STON1-GTF2A1L and Hypergonadotropic hypogonadism 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:11589532 (Homo sapiens)
  • 68 RGD objects have been annotated to Hypergonadotropic hypogonadism  (HP:0000815)
  • 2 papers in RGD have been used to annotate STON1-GTF2A1L
  • Curation Notes: ClinVar Annotator: match by term: Primary hypogonadism


    • An association has been curated linking STON1-GTF2A1L and Hypergonadotropic hypogonadism 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:11646703 (Homo sapiens)
  • 68 RGD objects have been annotated to Hypergonadotropic hypogonadism  (HP:0000815)
  • 2 papers in RGD have been used to annotate STON1-GTF2A1L
  • Curation Notes: ClinVar Annotator: match by term: Primary hypogonadism


    • An association has been curated linking STON1-GTF2A1L and Hypergonadotropic hypogonadism 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:11589711 (Homo sapiens)
  • 68 RGD objects have been annotated to Hypergonadotropic hypogonadism  (HP:0000815)
  • 2 papers in RGD have been used to annotate STON1-GTF2A1L
  • Curation Notes: ClinVar Annotator: match by term: Primary hypogonadism


    • An association has been curated linking STON1-GTF2A1L and Hypergonadotropic hypogonadism 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:11585434 (Homo sapiens)
  • 68 RGD objects have been annotated to Hypergonadotropic hypogonadism  (HP:0000815)
  • 2 papers in RGD have been used to annotate STON1-GTF2A1L
  • Curation Notes: ClinVar Annotator: match by term: Primary hypogonadism


    • An association has been curated linking STON1-GTF2A1L and Hypergonadotropic hypogonadism 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:11582988 (Homo sapiens)
  • 68 RGD objects have been annotated to Hypergonadotropic hypogonadism  (HP:0000815)
  • 2 papers in RGD have been used to annotate STON1-GTF2A1L
  • Curation Notes: ClinVar Annotator: match by term: Primary hypogonadism
  • Original References(s): PMID:28492532


    • An association has been curated linking STON1-GTF2A1L and Hypergonadotropic hypogonadism 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:11583795 (Homo sapiens)
  • 68 RGD objects have been annotated to Hypergonadotropic hypogonadism  (HP:0000815)
  • 2 papers in RGD have been used to annotate STON1-GTF2A1L
  • Curation Notes: ClinVar Annotator: match by term: Primary hypogonadism


    • An association has been curated linking STON1-GTF2A1L and Hypergonadotropic hypogonadism 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:11587510 (Homo sapiens)
  • 68 RGD objects have been annotated to Hypergonadotropic hypogonadism  (HP:0000815)
  • 2 papers in RGD have been used to annotate STON1-GTF2A1L
  • Curation Notes: ClinVar Annotator: match by term: Primary hypogonadism


    • An association has been curated linking STON1-GTF2A1L and Hypergonadotropic hypogonadism 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:11584493 (Homo sapiens)
  • 68 RGD objects have been annotated to Hypergonadotropic hypogonadism  (HP:0000815)
  • 2 papers in RGD have been used to annotate STON1-GTF2A1L
  • Curation Notes: ClinVar Annotator: match by term: Primary hypogonadism
  • Original References(s): PMID:28492532


    • An association has been curated linking STON1-GTF2A1L and Hypergonadotropic hypogonadism 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:11584548 (Homo sapiens)
  • 68 RGD objects have been annotated to Hypergonadotropic hypogonadism  (HP:0000815)
  • 2 papers in RGD have been used to annotate STON1-GTF2A1L
  • Curation Notes: ClinVar Annotator: match by term: Primary hypogonadism


    • An association has been curated linking STON1-GTF2A1L and Hypergonadotropic hypogonadism 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:11647689 (Homo sapiens)
  • 68 RGD objects have been annotated to Hypergonadotropic hypogonadism  (HP:0000815)
  • 2 papers in RGD have been used to annotate STON1-GTF2A1L
  • Curation Notes: ClinVar Annotator: match by term: Primary hypogonadism


    • An association has been curated linking STON1-GTF2A1L and Hypergonadotropic hypogonadism 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:11583229 (Homo sapiens)
  • 68 RGD objects have been annotated to Hypergonadotropic hypogonadism  (HP:0000815)
  • 2 papers in RGD have been used to annotate STON1-GTF2A1L
  • Curation Notes: ClinVar Annotator: match by term: Primary hypogonadism


    • An association has been curated linking STON1-GTF2A1L and Hypergonadotropic hypogonadism 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:11587791 (Homo sapiens)
  • 68 RGD objects have been annotated to Hypergonadotropic hypogonadism  (HP:0000815)
  • 2 papers in RGD have been used to annotate STON1-GTF2A1L
  • Curation Notes: ClinVar Annotator: match by term: Primary hypogonadism


    • An association has been curated linking STON1-GTF2A1L and Hypergonadotropic hypogonadism 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:11586166 (Homo sapiens)
  • 68 RGD objects have been annotated to Hypergonadotropic hypogonadism  (HP:0000815)
  • 2 papers in RGD have been used to annotate STON1-GTF2A1L
  • Curation Notes: ClinVar Annotator: match by term: Primary hypogonadism


    • An association has been curated linking STON1-GTF2A1L and Hypergonadotropic hypogonadism 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:11587541 (Homo sapiens)
  • 68 RGD objects have been annotated to Hypergonadotropic hypogonadism  (HP:0000815)
  • 2 papers in RGD have been used to annotate STON1-GTF2A1L
  • Curation Notes: ClinVar Annotator: match by term: Primary hypogonadism


    • An association has been curated linking STON1-GTF2A1L and Hypergonadotropic hypogonadism 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:11583614 (Homo sapiens)
  • 68 RGD objects have been annotated to Hypergonadotropic hypogonadism  (HP:0000815)
  • 2 papers in RGD have been used to annotate STON1-GTF2A1L
  • Curation Notes: ClinVar Annotator: match by term: Primary hypogonadism


    • An association has been curated linking STON1-GTF2A1L and Hypergonadotropic hypogonadism 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:11587217 (Homo sapiens)
  • 68 RGD objects have been annotated to Hypergonadotropic hypogonadism  (HP:0000815)
  • 2 papers in RGD have been used to annotate STON1-GTF2A1L
  • Curation Notes: ClinVar Annotator: match by term: Primary hypogonadism
  • Original References(s): PMID:28492532


    • An association has been curated linking STON1-GTF2A1L and Hypergonadotropic hypogonadism 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:11589412 (Homo sapiens)
  • 68 RGD objects have been annotated to Hypergonadotropic hypogonadism  (HP:0000815)
  • 2 papers in RGD have been used to annotate STON1-GTF2A1L
  • Curation Notes: ClinVar Annotator: match by term: Primary hypogonadism


    • An association has been curated linking STON1-GTF2A1L and Hypergonadotropic hypogonadism 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:11586408 (Homo sapiens)
  • 68 RGD objects have been annotated to Hypergonadotropic hypogonadism  (HP:0000815)
  • 2 papers in RGD have been used to annotate STON1-GTF2A1L
  • Curation Notes: ClinVar Annotator: match by term: Hypergonadotropic hypogonadism
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking STON1-GTF2A1L and Hypergonadotropic hypogonadism 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:11585294 (Homo sapiens)
  • 68 RGD objects have been annotated to Hypergonadotropic hypogonadism  (HP:0000815)
  • 2 papers in RGD have been used to annotate STON1-GTF2A1L
  • Curation Notes: ClinVar Annotator: match by term: Hypergonadotropic hypogonadism
  • Original References(s): PMID:25741868


    • An association has been curated linking STON1-GTF2A1L and Hypergonadotropic hypogonadism 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:11584132 (Homo sapiens)
  • 68 RGD objects have been annotated to Hypergonadotropic hypogonadism  (HP:0000815)
  • 2 papers in RGD have been used to annotate STON1-GTF2A1L
  • Curation Notes: ClinVar Annotator: match by term: Hypergonadotropic hypogonadism
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking STON1-GTF2A1L and Hypergonadotropic hypogonadism 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:11664788 (Homo sapiens)
  • 68 RGD objects have been annotated to Hypergonadotropic hypogonadism  (HP:0000815)
  • 2 papers in RGD have been used to annotate STON1-GTF2A1L
  • Curation Notes: ClinVar Annotator: match by term: Hypergonadotropic hypogonadism
  • Original References(s): PMID:12679452 PMID:2244890 PMID:26467025 PMID:28492532 PMID:7556872 PMID:9851790


    • An association has been curated linking STON1-GTF2A1L and Hypergonadotropic hypogonadism 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:11583518 (Homo sapiens)
  • 68 RGD objects have been annotated to Hypergonadotropic hypogonadism  (HP:0000815)
  • 2 papers in RGD have been used to annotate STON1-GTF2A1L
  • Curation Notes: ClinVar Annotator: match by term: Hypergonadotropic hypogonadism
  • Original References(s): PMID:25741868


    • An association has been curated linking STON1-GTF2A1L and Hypergonadotropic hypogonadism 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:11585480 (Homo sapiens)
  • 68 RGD objects have been annotated to Hypergonadotropic hypogonadism  (HP:0000815)
  • 2 papers in RGD have been used to annotate STON1-GTF2A1L
  • Curation Notes: ClinVar Annotator: match by term: Hypergonadotropic hypogonadism
  • Original References(s): PMID:28492532


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