/muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A5

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A5

Rare Disease

MONDO:0013157

Also Known As

muscle-eye-brain-FKRP relatedMDDGA5Walker-Warburg syndrome or muscle-eye-brain disease, FKRP-relatedmuscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5

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Associated Genes

FKRP ↗

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:613153 ↗

GARD

GARD:15625 ↗

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