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DO Term : thyroid dyshormonogenesis 4 [DOID:0112188] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A familial thyroid dyshormonogenesis that has_material_basis_in homozygous or compound heterozygous mutation in IYD on chromosome 6q25.1.

synonyms:
MESH:C562770,
iodotyrosine dehalogenase deficiency,
OMIM:274800,
genetic defect in thyroid hormonogenesis 4,
TDH4,
deiodinase deficiency,
274800

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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