|
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
Xenbase Genes
:
dnah11
| MONDO:0012748 - primary ciliary dyskinesia 7 |
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)