has material basis in autosomal recessive disease primary ciliary dyskinesia 42 A primary ciliary dyskinesia characterized by severe reduction or absence of multiple motile cilia in respiratory epithelia, onset of respiratory insufficiency soon after birth, recurrent upper and lower respiratory infections, and absence of laterality defects that has_material_basis_in homozygous or compound heterozygous mutation in the MCIDAS gene on chromosome 5q11.2. CILD42 disease_ontology MIM:618695 DOID:0111855 primary ciliary dyskinesia 42 without situs inversus primary ciliary dyskinesia autosomal recessive inheritance