oculocutaneous albinism type 2

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
oculocutaneous albinism type 2
OCA2 Unknown — ClinGen
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with oculocutaneous albinism type 2.
5 View disease cluster →
Brown oculocutaneous albinism 1 shared geneOCA2 Related via 1 shared gene including OCA2. Skin hair eye pigmentation variation 1 shared geneOCA2 Related via 1 shared gene including OCA2. Congenital nystagmus 1 shared geneOCA2 Related via 1 shared gene including OCA2. Prader-willi syndrome 1 shared geneOCA2 Related via 1 shared gene including OCA2. Angelman syndrome 1 shared geneOCA2 Related via 1 shared gene including OCA2.