Distal lower limb muscle weakness
Symptom Information:
Symptom ID: | HPO:0009053 | ||||
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) Distal muscle weakness(HPO:0002460) Distal lower limb muscle weakness(HPO:0009053) MedDRA: |
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Database Frequency: | 13 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Autosomal dominant Emery-Dreifuss muscular dystrophy | (Orphanet:98853) |
Autosomal recessive limb-girdle muscular dystrophy type 2G | (Orphanet:34514) |
Autosomal recessive spastic paraplegia type 39 | (Orphanet:139480) |
Autosomal recessive spastic paraplegia type 43 | (Orphanet:320370) |
Behr syndrome | (Orphanet:1239) |
Cap myopathy | (Orphanet:171881) |
Charcot-Marie-Tooth disease type 4H | (Orphanet:99954) |
Distal hereditary motor neuropathy type 2 | (Orphanet:139525) |
Distal spinal muscular atrophy type 3 | (Orphanet:139547) |
NEMALINE MYOPATHY 1 | (OMIM:609284) |
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIB | (OMIM:608634) |
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC | (OMIM:613376) |
X-linked Emery-Dreifuss muscular dystrophy | (Orphanet:98863) |