Generalized limb muscle atrophy
Symptom Information:
Symptom ID: | HPO:0009055 | |||
Synonyms: |
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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) Generalized amyotrophy(HPO:0003700) Generalized limb muscle atrophy(HPO:0009055) MedDRA: |
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Database Frequency: | 4 / 7739 | |||
Resource: |
All diseases associated with this symptom:
Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency | (Orphanet:329314) |
MYOPATHY, MYOSIN STORAGE | (OMIM:608358) |
McLeod neuroacanthocytosis syndrome | (Orphanet:59306) |
Myopathy, lactic acidosis, and sideroblastic anemia 1; MLASA1 | (OMIM:600462) |