Leber congenital amaurosis 15

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Subtype of: Leber congenital amaurosis
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Leber congenital amaurosis 15
MONDO_0018998
TULP1 Causal
15024725 17962469
ClinGen, Open Targets —
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Leber congenital amaurosis 15.
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Brachydactyly 1 shared geneTULP1 Related via 1 shared gene including TULP1. Syndactyly 1 shared geneTULP1 Related via 1 shared gene including TULP1. Stargardt disease 1 shared geneTULP1 Related via 1 shared gene including TULP1. Polydactyly 1 shared geneTULP1 Related via 1 shared gene including TULP1. Leber congenital amaurosis 1 shared geneTULP1 Related via 1 shared gene including TULP1.