Optic nerve hypoplasia and abnormalities of the central nervous system

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Optic nerve hypoplasia and abnormalities of the central nervous system
MONDO_0007400
SOX2 Unknown
19801978 16904174 21326281 7849401 16651659 17015430 17554336 8741917 19898493 16283891 16543359 18029452 24048479 15240551 12002146 16145681 21532573 17554338 18157115 18285410 19921648 20803647 18831064 18818365 19254784 21331042 15846349 17522155 12612584 16932809 19403656 15346919 16470798 12036291 16712695 16892407 18385377 21919124 10564870 17219395 12461687 15812812 15389708 18845712 18806776 11135495 17515932 30262714 14517545 24909994
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Optic nerve hypoplasia and abnormalities of the central nervous system.
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Microphthalmia, syndromic 3 1 shared geneSOX2 Related via 1 shared gene including SOX2. Microphthalmia syndromic type 3, optic nerve hypoplasia and abnormalities of the central nervous system 1 shared geneSOX2 Related via 1 shared gene including SOX2. Thoracic neoplasms 1 shared geneSOX2 Related via 1 shared gene including SOX2. Aniridia 1 shared geneSOX2 Related via 1 shared gene including SOX2. Sensorineural hearing loss 1 shared geneSOX2 Related via 1 shared gene including SOX2.