primary ciliary dyskinesia 32 disease_ontology DOID:0110603 ICD10CM:Q34.8 A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with near absence of radial spokes, respiratory distress in term neonates, impaired mucociliary clearance, chronic respiratory infections, bronchiectasis, and infertility and has_material_basis_in homozygous or compound heterozygous mutation in the RSPH3 gene on chromosome 6q25. CILD32 MIM:616481 primary ciliary dyskinesia 32 without situs inversus primary ciliary dyskinesia