DO_rare_slim has material basis in autosomal recessive disease primary ciliary dyskinesia 50 UMLS_CUI:C5830473 disease_ontology MIM:620356 DOID:0070763 MIM:620356 UMLS_CUI:C5830473 A primary ciliary dyskinesia characterized by chronic sinusitis, bronchitis, and male infertility with markedly reduced progressive motility and multiple morphologic abnormalities of the flagella resulting from defects or loss of the inner dynein arms of the sperm flagella that has_material_basis_in homozygous or compound heterozygous mutation in the DNAH7 gene on chromosome 2q32. CILD50 primary ciliary dyskinesia autosomal recessive inheritance