Brown oculocutaneous albinism

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
BROWN OCULOCUTANEOUS ALBINISM
C0268497
OCA2 Causal — Disgenet
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Brown oculocutaneous albinism.
5 View disease cluster →
oculocutaneous albinism type 2 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.