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DOID:0111850 - primary ciliary dyskinesia 36
Disease Ontology Definition:A primary ciliary dyskinesia characterized by absence of outer dynein arms, defects in inner dynein arms, chronic airway disease and recurrent sinopulmonary infections, male infertility, and laterality defects in about half of patients that has_material_basis_in hemizygous mutation in the PIH1D3 gene on chromosome Xq22.3.
Synonyms: CILD36, X-linked primary ciliary dyskinesia 36
Xenbase Genes
:
dnaaf6
| MIM:300991 - CILIARY DYSKINESIA, PRIMARY, 36, X-LINKED; CILD36 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
primary ciliary dyskinesia (is_a)