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DO Term : familial gestational hyperthyroidism [DOID:0081102] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A hyperthyroidism that is characterized by promiscuous stimulation of the thyrotropin receptor by the excess chorionic gonadotropin and that has_material_basis_in heterozygous mutation in the gene encoding the thyroid-stimulating hormone receptor (TSHR) on chromosome 14q31.
  • synonyms:
  • ORDO:99819,
  • 603373,
  • OMIM:603373
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents





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