| Term Name: | primary ciliary dyskinesia 52 |
|---|---|
| Synonyms: | CILD52 |
| Definition: | A primary ciliary dyskinesia characterized by laterality defects and mild respiratory symptoms due to subtle ciliary beating defects that has_material_basis_in homozygous or compound heterozygous mutation in the DAW1 gene on chromosome 2q36. |
| Ontology: | Human Disease [DOID:0070765] ( DOID:0070765 ) |