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DO Term : congenital nongoitrous hypothyroidism 1 [DOID:0070126] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A congenital hypothyroidism that has_material_basis_in mutation in the TSHR gene on chromosome 14q31.

synonyms:
ICD10CM:E03.1,
OMIM:275200,
275200,
TSH resistance,
CHNG1

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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