Proximal upper limb amyotrophy
Symptom Information:
Symptom ID: | HPO:0008948 | ||||
Synonyms: |
|
||||
Quality: | |||||
Cross references: |
|
||||
Is a (Direct Parents): |
|
||||
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) Proximal amyotrophy(HPO:0007126) Proximal upper limb amyotrophy(HPO:0008948) MedDRA: |
||||
Database Frequency: | 3 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Autosomal dominant limb-girdle muscular dystrophy type 1G | (Orphanet:55596) |
Autosomal recessive limb-girdle muscular dystrophy type 2B | (Orphanet:268) |
Autosomal recessive limb-girdle muscular dystrophy type 2G | (Orphanet:34514) |