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DO Term : primary ciliary dyskinesia 37 [DOID:0080266] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A primary ciliary dyskinesia that has_material_basis_in homozygous mutation in the DNAH1 gene on chromosome 3p21.

synonyms:
OMIM:617577,
617577

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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