congenital muscular dystrophy with intellectual disability and severe epilepsy

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
congenital muscular dystrophy with intellectual disability and severe epilepsy
DPM2 Causal — ClinGen
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with congenital muscular dystrophy with intellectual disability and severe epilepsy.
4 View disease cluster →
Primary angle closure glaucoma 1 shared geneDPM2 Related via 1 shared gene including DPM2. Congenital muscular dystrophy 1 shared geneDPM2 Related via 1 shared gene including DPM2. Congenital disorder of glycosylation 1 shared geneDPM2 Related via 1 shared gene including DPM2. Glaucoma 1 shared geneDPM2 Related via 1 shared gene including DPM2.