primary ciliary dyskinesia 17 MIM:614679 ICD10CM:Q34.8 A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with inner and outer dynein arm defect, early infantile onset of respiratory distress, and variable occurence of laterality defects and has_material_basis_in homozygous mutation in the CCDC103 gene on chromosome 17q21. DOID:0110621 CILD17 disease_ontology primary ciliary dyskinesia 17 with or without situs inversus primary ciliary dyskinesia