Term Name: primary ciliary dyskinesia 48
Synonyms: CILD48
Definition: A primary ciliary dyskinesia characterized by recurrent upper and lower respiratory infections due to impaired ciliary movement and clearance, resulting from defects in the radial spokes and central pairs of microtubules in motile cilia that has_material_basis_in homozygous mutation in the NME5 gene on chromosome 5q31. Situs abnormalities have not been reported.
Ontology: Human Disease [DOID:0070761]   ( DOID:0070761 )

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