Upper limb muscle weakness
Symptom Information:
| Symptom ID: | HPO:0003484 | ||
| 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 physiology(HPO:0011804) Muscle weakness(HPO:0001324) Limb muscle weakness(HPO:0003690) Upper limb muscle weakness(HPO:0003484) MedDRA: |
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| Database Frequency: | 19 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| Autosomal dominant Charcot-Marie-Tooth disease type 2D | (Orphanet:99938) |
| Autosomal dominant Charcot-Marie-Tooth disease type 2I | (Orphanet:99942) |
| Autosomal dominant intermediate Charcot-Marie-Tooth disease type C | (Orphanet:100045) |
| Autosomal dominant intermediate Charcot-Marie-Tooth disease type D | (Orphanet:100046) |
| Autosomal recessive limb-girdle muscular dystrophy type 2B | (Orphanet:268) |
| Autosomal recessive spastic paraplegia type 7 | (Orphanet:99013) |
| Carbamoylphosphate synthetase deficiency | (Orphanet:147) |
| Charcot-Marie-Tooth disease type 1D | (Orphanet:101084) |
| Charcot-Marie-Tooth disease type 2B1 | (Orphanet:98856) |
| Charcot-Marie-Tooth disease type 4C | (Orphanet:99949) |
| Charcot-Marie-Tooth disease type 4E | (Orphanet:99951) |
| Charcot-Marie-Tooth disease type 4H | (Orphanet:99954) |
| Distal hereditary motor neuropathy type 1 | (Orphanet:139518) |
| Distal hereditary motor neuropathy type 5 | (Orphanet:139536) |
| Monomelic amyotrophy | (Orphanet:65684) |
| Primary hyperoxaluria type 1 | (Orphanet:93598) |
| Pyruvate dehydrogenase E1-alpha deficiency | (Orphanet:79243) |
| X-linked Charcot-Marie-Tooth disease type 2 | (Orphanet:101076) |
| X-linked Charcot-Marie-Tooth disease type 3 | (Orphanet:101077) |