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DO Term : thyroid dyshormonogenesis 5 [DOID:0112184] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A familial thyroid dyshormonogenesis that has_material_basis_in homozygous or compound heterozygous mutation in DUOXA2 on chromosome 15q21.1.

synonyms:
OMIM:274900,
274900,
TDH5,
genetic defect in thyroid hormonogenesis 5,
MESH:C562771

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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