has material basis in autosomal dominant disease primary ciliary dyskinesia 43 MIM:618699 DOID:0111856 A primary ciliary dyskinesia characterized by reduced generation of multiple motile cilia, onset of respiratory insufficiency soon after birth, recurrent upper and lower respiratory infections,variable infertility, and laterality defects in about half of patients that has_material_basis_in heterozygous mutation in FOXJ1 on chromosome 17q25.1. CILD43 disease_ontology primary ciliary dyskinesia 43 with or without situs inversus primary ciliary dyskinesia autosomal dominant inheritance