Human genes for Keipert syndrome
Keipert syndrome [DOID:0111842]
A syndrome characterized by craniofacial and digital abnormalities, mild to severe congenital sensorineural hearing loss, and variable learning difficulties that has_material_basis_in hemizygous mutation in GPC4 on chromosome Xq26.2.
Synonyms: Keipert syndrome, DOID:0111842, Keipert disease, Keipert disorder, Keipert syndromes ...