primary ciliary dyskinesia 15 (DOID:0110623)
Alliance: disease page
Synonyms: CILD15; primary ciliary dyskinesia 15 with or without situs inversus
Alt IDs: OMIM:613808, ICD10CM:Q34.8
Definition: A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with inner dynein arm defect, axonemal disorganization, recurrent respiratory infections and has_material_basis_in homozygous or compound heterozygous mutation in the CCDC40 gene on chromosome 17q25.