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DO Term : congenital nongoitrous hypothyroidism 9 [DOID:0111835] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A congenital hypothyroidism characterized by a small thyroid gland with low free T4 levels and inappropriately normal levels of thyroid-stimulating hormone that has_material_basis_in hemizygous mutation in the IRS4 gene on chromosome Xq22.3.
  • synonyms:
  • OMIM:301035,
  • 301035,
  • CHNG9
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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