Abnormality of the eye

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Abnormality of the eye
HP:0000478
MAB21L1 Unknown
30487245 27103078
Open Targets —
MED13 Unknown
29740699
Open Targets
P4HTM Unknown
25078763 30940925
Open Targets —
All3 Causal0 Unknown3
Related Diseases Diseases that share the most curated genes with Abnormality of the eye.
5 View disease cluster →
Intellectual developmental disorder, autosomal dominant 61 1 shared geneMED13 Related via 1 shared gene including MED13. Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome 1 shared geneMAB21L1 Related via 1 shared gene including MAB21L1. Cerebello-oculo-facio-genital syndrome 1 shared geneMAB21L1 Related via 1 shared gene including MAB21L1. Hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities 1 shared geneP4HTM Related via 1 shared gene including P4HTM. Hypoventilation 1 shared geneP4HTM Related via 1 shared gene including P4HTM.