primary ciliary dyskinesia 26 disease_ontology MIM:615500 ICD10CM:Q34.8 A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with inner and outer dynein arm defect, neonatal respiratory distress, recurrent upper and lower airway disease, bronchiectasis, and variable occurence of laterality defects and has_material_basis_in homozygous or compound heterozygous mutation in the C21ORF59 gene on chromosome 21q22. CILD26 DOID:0110627 primary ciliary dyskinesia 26 with or without situs inversus primary ciliary dyskinesia