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DO Term : autosomal dominant woolly hair [DOID:0111573] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A familial woolly hair syndrome that has_material_basis_in heterozygous mutation in the KRT74 gene on chromosome 12q13.13.

synonyms:
ADWH,
194300,
SNOMEDCT_US_2022_07_31:403794008,
OMIM:194300

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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