Human genes for Nance-Horan syndrome
Nance-Horan syndrome [DOID:0060599]
A syndrome that has_material_basis_in mutation in the NHS gene on chromosome Xp22 and is characterized by congenital cataract leading to profound vision loss, characteristic dysmorphic features and dental anomalies.
Synonyms: Nance-Horan syndrome, DOID:0060599, NanceHoran syndrome, Nance-Horan disease, Nance-Horan disorder ...