Hypoglycosylation of alpha-dystroglycan seen on muscle biopsy
Symptom Information:
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Symptom ID:
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OMIM : No Id available
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Synonyms:
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Quality:
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Cross references:
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| OMIM: "Hypoglycosylation of alpha-dystroglycan seen on muscle biopsy" [OMIM:Hypoglycosylation of alpha-dystroglycan seen on muscle biopsy] |
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Is a (Direct Parents):
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Is a (Whole tree):
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HPO:
MedDRA:
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Database Frequency:
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3 / 7739
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Resource:
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All diseases associated with this symptom:
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Autosomal recessive limb-girdle muscular dystrophy type 2P
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(Orphanet:280333)
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MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 14
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(OMIM:615350)
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MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 14
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(OMIM:615351)
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