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RGD uses the Human Disease Ontology (DO, for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.

Term:Familial Gestational Hyperthyroidism
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Accession:DOID:9000010 term browser browse the term
Synonyms:primary_id: MESH:C566384
 alt_id: OMIM:603373
For additional species annotation, visit the Alliance of Genome Resources.

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Familial Gestational Hyperthyroidism term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Tshr thyroid stimulating hormone receptor ISO ClinVar Annotator: match by term: Hyperthyroidism, familial gestational OMIM
PMID:25741868 NCBI chr 6:110,341,585...110,475,297
Ensembl chr 6:110,341,581...110,474,538
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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 17205
    disease of anatomical entity 16551
      Urogenital Diseases 4356
        Female Urogenital Diseases and Pregnancy Complications 2044
          Pregnancy Complications 573
            Familial Gestational Hyperthyroidism 1
paths to the root