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DO Term : primary ciliary dyskinesia 6 [DOID:0110606] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A primary ciliary dyskinesia that is characterized by partial outer dynein arm defect and has_material_basis_in mutation in the TXNDC3 gene on the chromosome 7p14.1.

synonyms:
610852,
ICD10CM:Q34.8,
OMIM:610852,
CILD6

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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