primary ciliary dyskinesia 35 disease_ontology DOID:0110620 MIM:617092 A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with absent outer dynein arms, immotile cilia, variable occurence of laterality defects and recurrent upper and lower respiratory infections and has_material_basis_in homozygous mutation in the TTC25 gene on chromosome 17q21. CILD35 primary ciliary dyskinesia 35 with or without situs inversus primary ciliary dyskinesia