DO_rare_slim has material basis in autosomal recessive disease primary ciliary dyskinesia 51 UMLS_CUI:C5830608 A primary ciliary dyskinesia characterized by male infertility with markedly reduced progressive motility and multiple morphologic abnormalities of the flagella, chronic rhinosinusitis and bronchitis, and recurrent upper and lower respiratory infections that has_material_basis_in homozygous or compound heterozygous mutation in the BRWD1 gene on chromosome 21q22. Situs abnormalities have been reported. MIM:620438 MIM:620438 CILD51 disease_ontology DOID:0070764 UMLS_CUI:C5830608 primary ciliary dyskinesia autosomal recessive inheritance