DISEASES

Disease-gene associations mined from literature

Human genes for congenital nystagmus

Congenital nystagmus [DOID:9649]

Nystagmus /nɪˈstæɡməs/ is a condition of involuntary eye movement, acquired in infancy or later in life, that may result in reduced or limited vision.

Synonyms:  congenital nystagmus,  DOID:9649

Linkouts:  OMIM #1 #2 #3 #4 #5 #6 #7 #8 #9 #10 #11