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myopathy, epilepsy, and progressive cerebral atrophy | RareConnect | RareConnect.io

/ALG14-congenital disorder of glycosylation

/myopathy, epilepsy, and progressive cerebral atrophy

myopathy, epilepsy, and progressive cerebral atrophy

Rare Disease

MONDO:0033619

Also Known As

MEPCA

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

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Associated Genes

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

External Resources

OMIM

OMIM:619036 ↗

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