Human genes for primary ciliary dyskinesia 7
Primary ciliary dyskinesia 7 [DOID:0110605]
A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with chronic respiratory infections, chronic sinusitis, recurrent bronchitis, and pneumonia beginning in infancy or early childhood and has_material_basis_in mutation in the DNAH11 gene on chromosome 7p21.
Synonyms: primary ciliary dyskinesia 7, DOID:0110605, CILD7, primary ciliary dyskinesia 7 with or without situs inversus