Disease-gene associations mined from literature

Human genes for vitreoretinal dystrophy

Vitreoretinal dystrophy [DOID:14251]

A neonatal period electroclinical syndrome that is characterized by tonic-clonic seizures in newborns occurring within the first seven days of life and ceasing within the first 15 weeks of life and has_material_basis_in autosomal dominant inheritance of voltage-gated potassium channels or a chromosomal inversion.

Synonyms:  vitreoretinal dystrophy,  DOID:14251,  Vitreoretinal dystrophies,  Vitreoretinal dystrophy (disorder),  Vitreoretinal dystrophy