primary ciliary dyskinesia 5 (DOID:0110617)
Alliance: disease page
Synonyms: CILD5; primary ciliary dyskinesia 5 without situs inversus
Alt IDs: OMIM:608647, ICD10CM:Q34.8
Definition: A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with early onset of a progressive decline in lung function and has_material_basis_in homozygous mutation in the HYDIN gene on chromosome 16q22.