Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type b15

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Subtype of: Congenital muscular dystrophy due to dystroglycanopathy · Muscular dystrophy
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Pathways column key: KEGG Reactome
Disease terms Disease ID Gene Symbol Classification References Source Pathways
  • muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type b, 15
MONDO_0033556
DPM3 Causal
19576565 28803818 31266720
Open Targets
All1 Causal1 Unknown1
Related Diseases Diseases that share the most curated genes with Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type b15.
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Limb-girdle muscular dystrophy 1 shared geneDPM3 Related via 1 shared gene including DPM3. Congenital disorder of glycosylation 1 shared geneDPM3 Related via 1 shared gene including DPM3. Myopathy 1 shared geneDPM3 Related via 1 shared gene including DPM3. Cardiomyopathy 1 shared geneDPM3 Related via 1 shared gene including DPM3. Gout 1 shared geneDPM3 Related via 1 shared gene including DPM3.