primary ciliary dyskinesia 18 DOID:0110604 MIM:614874 disease_ontology ICD10CM:Q34.8 A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with outer and inner dynein arm defect, early infantile onset of recurrent sinopulmonary infections, male infertility, and variable occurence of situs inversus and has_material_basis_in homozygous mutation in the HEATR2 gene on chromosome 7p22. CILD18 primary ciliary dyskinesia 18 with or without situs inversus primary ciliary dyskinesia