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Collaborative Research
Diseases
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Nervous system disorder
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Hereditary neurological disease
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Hereditary neuromuscular disease
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DPM3-congenital disorder of glycosylation
Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 15
rare
Identifiers
MONDO:0033556
OMIM:618992
Part of
DPM3-congenital disorder of glycosylation
Muscular dystrophy-dystroglycanopathy, type B
Also known as
MDDGB15
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