DOID:0110605 - primary ciliary dyskinesia 7
Disease Ontology Definition:A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with chronic respiratory infections, chronic sinusitis, recurrent bronchitis, and pneumonia beginning in infancy or early childhood and has_material_basis_in mutation in the DNAH11 gene on chromosome 7p21.
Synonyms: CILD7; primary ciliary dyskinesia 7 with or without situs inversus
|OMIM:611884 - CILIARY DYSKINESIA, PRIMARY, 7; CILD7|
Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Xenbase Genes : dnah11
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): primary ciliary dyskinesia (is_a)