primary ciliary dyskinesia 35

Summary

DOID:0110620 - primary ciliary dyskinesia 35

Disease Ontology Definition:A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with absent outer dynein arms, immotile cilia, variable occurence of laterality defects and recurrent upper and lower respiratory infections and has_material_basis_in homozygous mutation in the TTC25 gene on chromosome 17q21.

Synonyms: CILD35, primary ciliary dyskinesia 35 with or without situs inversus

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: odad4

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014910 - primary ciliary dyskinesia 35

MONDO:0014910 - primary ciliary dyskinesia 35

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)