Myopia 27, autosomal dominant

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Subtype of: Myopia
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Myopia 27, autosomal dominant
MONDO_0032941
CPSF1 Unknown
30689892
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Myopia 27, autosomal dominant.
3 View disease cluster →
Myopia 1 shared geneCPSF1 Related via 1 shared gene including CPSF1. Stomach neoplasms 1 shared geneCPSF1 Related via 1 shared gene including CPSF1. Retinitis pigmentosa 1 shared geneCPSF1 Related via 1 shared gene including CPSF1.