Lower limb amyotrophy
Symptom Information:
| Symptom ID: | HPO:0007210 | ||
| Synonyms: |
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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) Lower limb amyotrophy(HPO:0007210) MedDRA: |
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| Database Frequency: | 7 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| Autosomal dominant spastic paraplegia type 10 | (Orphanet:100991) |
| Autosomal dominant spastic paraplegia type 6 | (Orphanet:100988) |
| Autosomal recessive limb-girdle muscular dystrophy type 2G | (Orphanet:34514) |
| Autosomal recessive spastic paraplegia type 30 | (Orphanet:101010) |
| Friedreich ataxia 1 | (OMIM:229300) |
| Hypomyelination - congenital cataract | (Orphanet:85163) |
| X-linked spastic paraplegia type 16 | (Orphanet:100997) |