Congenital alpha-dystroglycanopathy with brain and eye anomalies

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Pathways column key: KEGG Reactome
Disease terms Disease ID Gene Symbol Classification References Source Pathways
  • congenital alpha-dystroglycanopathy with brain and eye anomalies
MONDO_0013157
FKRP Unknown
11053680 11071142 11592034 11741828 12654965 12707439 14523375 14647208 14652796 15121789 17336067 24139536 26833294
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Congenital alpha-dystroglycanopathy with brain and eye anomalies.
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Myopathy caused by variation in FKRP 1 shared geneFKRP Related via 1 shared gene including FKRP. Muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type b5 1 shared geneFKRP Related via 1 shared gene including FKRP. Paresthesia 1 shared geneFKRP Related via 1 shared gene including FKRP. Congenital muscular dystrophy due to dystroglycanopathy 1 shared geneFKRP Related via 1 shared gene including FKRP. Muscle eye brain disease 1 shared geneFKRP Related via 1 shared gene including FKRP.