has symptom primary ciliary dyskinesia 22 A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with outer and inner dynein arm defect, recurrent respiratory infections, persistent rhinosinusitis, otitis media, chronic cough, variable presence of situs abnormalities, and has_material_basis_in homozygous or compound heterozygous mutation in the ZMYND10 gene on chromosome 3p21. CILD22 MIM:615444 disease_ontology ICD10CM:Q34.8 DOID:0110597 primary ciliary dyskinesia 22 with or without situs inversus primary ciliary dyskinesia chronic cough