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Summary Literature (0)
DOID:0110608 - primary ciliary dyskinesia 19

Disease Ontology Definition:A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with outer and inner dynein arm defect, chronic sinopulmonary infections, asthenospermia, and immotile cilia and has_material_basis_in homozygous mutation in the LRRC6 gene on chromosome 8q24.

Synonyms: CILD19, primary ciliary dyskinesia 19 with or without situs inversus

Xenbase Genes : dnaaf11

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013979 - primary ciliary dyskinesia 19


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)