Upper limb amyotrophy
Symptom Information:
Symptom ID: | HPO:0009129 | ||||
Synonyms: |
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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) Upper limb amyotrophy(HPO:0009129) Abnormality of the skeletal system(HPO:0000924) Abnormality of skeletal morphology(HPO:0011842) Abnormal appendicular skeleton morphology(HPO:0011844) Abnormality of limb bone morphology(HPO:0002813) Abnormality of the upper limb(HPO:0002817) Upper limb amyotrophy(HPO:0009129) MedDRA: |
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Database Frequency: | 3 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Autosomal dominant Charcot-Marie-Tooth disease type 2D | (Orphanet:99938) |
Autosomal dominant spastic paraplegia type 10 | (Orphanet:100991) |
Friedreich ataxia 1 | (OMIM:229300) |