Term Name: primary ciliary dyskinesia 28
Synonyms: CILD28, primary ciliary dyskinesia 28 with or without situs inversus
Definition: A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with outer and inner dynein arm defect, recurrent upper and lower airway disease, bronchiectasis, and decreased fertility and has_material_basis_in homozygous or compound heterozygous mutation in the SPAG1 gene on chromosome 8q22.
Ontology: Human Disease [DOID:0110607]   ( DOID:0110607 )

Relationships
is a type of: primary ciliary dyskinesia