Human genes for primary ciliary dyskinesia 29
Primary ciliary dyskinesia 29 [DOID:0110600]
A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with oligocilia and early childhood onset of recurrent respiratory infections, and has_material_basis_in homozygous or compound heterozygous mutation in the CCNO gene on chromosome 5p15.
Synonyms: primary ciliary dyskinesia 29, DOID:0110600, CILD29, primary ciliary dyskinesia 29 without situs inversus