Proximal muscle weakness in lower limbs
Symptom Information:
Symptom ID: | HPO:0008994 | ||||
Synonyms: |
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Quality: | |||||
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 physiology(HPO:0011804) Muscle weakness(HPO:0001324) Proximal muscle weakness(HPO:0003701) Proximal muscle weakness in lower limbs(HPO:0008994) MedDRA: |
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Database Frequency: | 11 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Autosomal dominant Emery-Dreifuss muscular dystrophy | (Orphanet:98853) |
Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures | (Orphanet:209341) |
Autosomal dominant spastic paraplegia type 41 | (Orphanet:320355) |
Autosomal recessive limb girdle muscular dystrophy type 2A | (Orphanet:267) |
Autosomal recessive limb-girdle muscular dystrophy type 2G | (Orphanet:34514) |
Autosomal recessive limb-girdle muscular dystrophy type 2I | (Orphanet:34515) |
Becker muscular dystrophy | (Orphanet:98895) |
Duchenne muscular dystrophy | (Orphanet:98896) |
Proximal spinal muscular atrophy | (Orphanet:70) |
X-linked Emery-Dreifuss muscular dystrophy | (Orphanet:98863) |
X-linked myopathy with excessive autophagy | (Orphanet:25980) |