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muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 8 | RareConnect | RareConnect.io

/muscular dystrophy-dystroglycanopathy, type C

/autosomal recessive limb-girdle muscular dystrophy

/congenital muscular dystrophy caused by variation in POMGNT2

/muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 8

muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 8

Rare Disease

MONDO:0029135

Also Known As

LGMD-POMGNT2 related myopathymuscular dystrophy-dystroglycanopathy (limb-girdle) type C, 8MDDGC8Muscular dystrophy-dystroglycanopathy, limb-girdle, POMGNT2-relatedmuscular dystrophy, limb-girdle, autosomal recessive 24muscular dystrophy-dystroglycanopathy (limb-girdle), TYPE C, 8

Patient-Friendly Information

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Associated Genes

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

External Resources

OMIM

OMIM:618135 ↗

GARD

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