DISEASES

Disease-gene associations mined from literature

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