DISEASES

Disease-gene associations mined from literature

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Human genes for congenital nystagmus

Congenital nystagmus [DOID:9649]

A pathologic nystagmus, present at birth, characterized by involuntary, rhythmic eye movements; oscillations are usually horizontal in direction.

Synonyms:  congenital nystagmus,  DOID:9649,  congenital nystagmuses,  congenital nystagmi

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

The disease-gene associations are derived from automatic text mining of the biomedical literature, manually curated database annotations, cancer mutation data, and genome-wide association studies. The confidence of each association is signified by stars, where ★★★★★ is the highest confidence and ★☆☆☆☆ is the lowest.

Developed by Sune Frankild, Alexander Junge, Albert Pallejà, Dhouha Grissa, Kalliopi Tsafou, and Lars Juhl Jensen from the Novo Nordisk Foundation Center for Protein Research.