DISEASES

Disease-gene associations mined from literature

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