DISEASES

Disease-gene associations mined from literature

Human genes for Nance-Horan syndrome

Nance-Horan syndrome [DOID:0060599]

A X-linked dominant disease 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 ...