Limb-girdle muscle atrophy
Symptom Information:
Symptom ID: | HPO:0003797 | ||
Synonyms: |
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Quality: | |||
Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the musculature(HPO:0003011) Abnormality of muscle morphology(HPO:0011805) Skeletal muscle atrophy(HPO:0003202) Limb-girdle muscle atrophy(HPO:0003797) MedDRA: |
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Database Frequency: | 8 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Autosomal recessive Emery-Dreifuss muscular dystrophy | (Orphanet:98855) |
Autosomal recessive limb girdle muscular dystrophy type 2A | (Orphanet:267) |
Autosomal recessive limb-girdle muscular dystrophy type 2D | (Orphanet:62) |
Becker muscular dystrophy | (Orphanet:98895) |
Distal myopathy, Nonaka type | (Orphanet:602) |
Glycogen storage disease due to acid maltase deficiency, late-onset | (Orphanet:420429) |
INCLUSION BODY MYOPATHY 2, AUTOSOMAL RECESSIVE | (OMIM:600737) |
MYOPATHY WITH GIANT ABNORMAL MITOCHONDRIA | (OMIM:255140) |