Myopia 21, 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 21, autosomal dominant
MONDO_0001384
ZNF644 Causal
22539872 25525168 24991186 21695231
Open Targets —
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Myopia 21, autosomal dominant.
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Myopia 1 shared geneZNF644 Related via 1 shared gene including ZNF644. Kidney failure 1 shared geneZNF644 Related via 1 shared gene including ZNF644. Retinitis pigmentosa 1 shared geneZNF644 Related via 1 shared gene including ZNF644. Metabolic syndrome 1 shared geneZNF644 Related via 1 shared gene including ZNF644. Diabetes mellitus type 2 1 shared geneZNF644 Related via 1 shared gene including ZNF644.