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 )

Relationships
is a type of: autosomal recessive disease primary ciliary dyskinesia