Lower limb muscle weakness
Symptom Information:
Symptom ID: | HPO:0007340 | ||||||||||||||
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) Limb muscle weakness(HPO:0003690) Lower limb muscle weakness(HPO:0007340) MedDRA: |
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Database Frequency: | 61 / 7739 | ||||||||||||||
Resource: |
All diseases associated with this symptom:
Acute interstitial pneumonia | (Orphanet:79126) |
Autosomal dominant spastic paraplegia type 10 | (Orphanet:100991) |
Autosomal dominant spastic paraplegia type 12 | (Orphanet:100993) |
Autosomal dominant spastic paraplegia type 13 | (Orphanet:100994) |
Autosomal dominant spastic paraplegia type 17 | (Orphanet:100998) |
Autosomal dominant spastic paraplegia type 19 | (Orphanet:100999) |
Autosomal dominant spastic paraplegia type 3 | (Orphanet:100984) |
Autosomal dominant spastic paraplegia type 31 | (Orphanet:101011) |
Autosomal dominant spastic paraplegia type 36 | (Orphanet:320365) |
Autosomal dominant spastic paraplegia type 38 | (Orphanet:171617) |
Autosomal dominant spastic paraplegia type 4 | (Orphanet:100985) |
Autosomal dominant spastic paraplegia type 41 | (Orphanet:320355) |
Autosomal dominant spastic paraplegia type 42 | (Orphanet:171863) |
Autosomal dominant spastic paraplegia type 6 | (Orphanet:100988) |
Autosomal dominant spastic paraplegia type 8 | (Orphanet:100989) |
Autosomal dominant spastic paraplegia type 9 | (Orphanet:100990) |
Autosomal recessive Emery-Dreifuss muscular dystrophy | (Orphanet:98855) |
Autosomal recessive limb-girdle muscular dystrophy type 2B | (Orphanet:268) |
Autosomal recessive spastic paraplegia type 11 | (Orphanet:2822) |
Autosomal recessive spastic paraplegia type 14 | (Orphanet:100995) |
Autosomal recessive spastic paraplegia type 15 | (Orphanet:100996) |
Autosomal recessive spastic paraplegia type 18 | (Orphanet:209951) |
Autosomal recessive spastic paraplegia type 20 | (Orphanet:101000) |
Autosomal recessive spastic paraplegia type 21 | (Orphanet:101001) |
Autosomal recessive spastic paraplegia type 23 | (Orphanet:101003) |
Autosomal recessive spastic paraplegia type 28 | (Orphanet:101008) |
Autosomal recessive spastic paraplegia type 30 | (Orphanet:101010) |
Autosomal recessive spastic paraplegia type 32 | (Orphanet:171622) |
Autosomal recessive spastic paraplegia type 46 | (Orphanet:320391) |
Autosomal recessive spastic paraplegia type 48 | (Orphanet:306511) |
Autosomal recessive spastic paraplegia type 54 | (Orphanet:320380) |
Autosomal recessive spastic paraplegia type 55 | (Orphanet:320375) |
Autosomal recessive spastic paraplegia type 5A | (Orphanet:100986) |
Autosomal recessive spastic paraplegia type 7 | (Orphanet:99013) |
Beta-mannosidosis | (Orphanet:118) |
CEREBRAL SCLEROSIS, DIFFUSE, SCHOLZ TYPE | (OMIM:302700) |
Friedreich ataxia 1 | (OMIM:229300) |
Gerstmann-Straussler-Scheinker syndrome | (Orphanet:356) |
Hurler-Scheie syndrome | (Orphanet:93476) |
Hyperornithinemia-hyperammonemia-homocitrullinuria | (Orphanet:415) |
Hypomyelination - congenital cataract | (Orphanet:85163) |
MIYOSHI MUSCULAR DYSTROPHY 1 | (OMIM:254130) |
McLeod neuroacanthocytosis syndrome | (Orphanet:59306) |
Mitochondrial DNA deletion syndrome with progressive myopathy | (Orphanet:352470) |
Miyoshi myopathy | (Orphanet:45448) |
NEUROFIBROMATOSIS, FAMILIAL SPINAL | (OMIM:162210) |
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IID | (OMIM:615575) |
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIB | (OMIM:607641) |
NEUROPATHY, PAINFUL | (OMIM:256870) |
PARTIAL LIPODYSTROPHY, CONGENITAL CATARACTS, AND NEURODEGENERATIONSYNDROME | (OMIM:606721) |
Primary hyperoxaluria type 1 | (Orphanet:93598) |
Pyruvate dehydrogenase E1-alpha deficiency | (Orphanet:79243) |
SCAPULOPERONEAL MYOPATHY, X-LINKED DOMINANT | (OMIM:300695) |
SPASTIC PARAPLEGIA, ATAXIA, AND MENTAL RETARDATION | (OMIM:607565) |
Scheie syndrome | (Orphanet:93474) |
Spastic paraplegia - epilepsy - intellectual deficit | (Orphanet:2816) |
Spastic paraplegia 33, autosomal dominant | (OMIM:610244) |
Spastic paraplegia type 2 | (Orphanet:99015) |
Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers | (Orphanet:206546) |
X-linked spastic paraplegia type 16 | (Orphanet:100997) |
[DEL] SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE | (OMIM:607259) |