Term Name: primary ciliary dyskinesia 12
Synonyms: CILD12, primary ciliary dyskinesia 12 without situs inversus
Definition: A primary ciliary dyskinesia that is characterized by reduced exercise tolerance, chronic wet cough, recurrent respiratory infections, bronchiectasis, and nasal symptoms, and has_material_basis_in homozygous mutation in the RSPH9 gene on chromosome 6p21.
Ontology: Human Disease [DOID:0110601]   ( DOID:0110601 )

Relationships
is a type of: primary ciliary dyskinesia