Retinal dystrophy, early-onset, with or without pituitary dysfunction

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Subtype of: Retinal dystrophy
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Retinal dystrophy, early-onset, with or without pituitary dysfunction
MONDO_0012413
OTX2 Unknown
25293953 19956411
Open Targets —
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Retinal dystrophy, early-onset, with or without pituitary dysfunction.
5 View disease cluster →
Agnathia-holoprosencephaly-situs inversus syndrome 1 shared geneOTX2 Related via 1 shared gene including OTX2. Microphthalmia, syndromic 5 1 shared geneOTX2 Related via 1 shared gene including OTX2. Ectopic posterior pituitary 1 shared geneOTX2 Related via 1 shared gene including OTX2. Patterned macular dystrophy 1 shared geneOTX2 Related via 1 shared gene including OTX2. Butterfly-shaped pigmentary macular dystrophy 1 shared geneOTX2 Related via 1 shared gene including OTX2.