DO_rare_slim has material basis in autosomal recessive disease primary ciliary dyskinesia 49 UMLS_CUI:C5774291 A primary ciliary dyskinesia characterized by onset of recurrent respiratory infections, chronic cough, and bronchiectasis in early childhood due to defective ciliary clearance and male infertility due to defective flagellar morphology and function that has_material_basis_in compound heterozygous mutation in the CFAP74 gene on chromosome 1p36. Situs abnormalities have not been reported. disease_ontology UMLS_CUI:C5774291 MIM:620197 DOID:0070762 MIM:620197 CILD49 primary ciliary dyskinesia autosomal recessive inheritance