Lower limb spasticity
Symptom Information:
Symptom ID: | HPO:0002061 | ||
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 nervous system(HPO:0000707) Abnormality of nervous system physiology(HPO:0012638) Abnormality of central motor function(HPO:0011442) Abnormal pyramidal signs(HPO:0007256) Hypertonia(HPO:0001276) Spasticity(HPO:0001257) Lower limb spasticity(HPO:0002061) MedDRA: |
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Database Frequency: | 56 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Adult polyglucosan body disease | (Orphanet:206583) |
Argininemia | (Orphanet:90) |
Arnold-Chiari malformation type I | (Orphanet:268882) |
Ataxia-telangiectasia-like disorder | (Orphanet:251347) |
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 29 | (Orphanet:101009) |
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 37 | (Orphanet:171612) |
Autosomal dominant spastic paraplegia type 38 | (Orphanet:171617) |
Autosomal dominant spastic paraplegia type 4 | (Orphanet:100985) |
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 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 26 | (Orphanet:101006) |
Autosomal recessive spastic paraplegia type 27 | (Orphanet:101007) |
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 35 | (Orphanet:171629) |
Autosomal recessive spastic paraplegia type 44 | (Orphanet:320401) |
Autosomal recessive spastic paraplegia type 45 | (Orphanet:320396) |
Autosomal recessive spastic paraplegia type 46 | (Orphanet:320391) |
Autosomal recessive spastic paraplegia type 48 | (Orphanet:306511) |
Autosomal recessive spastic paraplegia type 5A | (Orphanet:100986) |
Autosomal recessive spastic paraplegia type 7 | (Orphanet:99013) |
Combined oxidative phosphorylation defect type 15 | (Orphanet:319524) |
Hereditary sensory and autonomic neuropathy with spastic paraplegia | (Orphanet:139578) |
Hurler-Scheie syndrome | (Orphanet:93476) |
Hyperornithinemia-hyperammonemia-homocitrullinuria | (Orphanet:415) |
Juvenile amyotrophic lateral sclerosis | (Orphanet:300605) |
MASA syndrome | (Orphanet:2466) |
PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE EARLY-ONSET | (OMIM:260300) |
Partington syndrome | (Orphanet:94083) |
Perrault Syndrome | (Orphanet:2855) |
Perrault Syndrome 3 | (OMIM:614129) |
Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
Pontocerebellar hypoplasia type 6 | (Orphanet:166073) |
Purine nucleoside phosphorylase deficiency | (Orphanet:760) |
SPASTIC PARAPLEGIA, ATAXIA, AND MENTAL RETARDATION | (OMIM:607565) |
Spastic paraplegia 33, autosomal dominant | (OMIM:610244) |
Spastic paraplegia 64, autosomal recessive | (OMIM:615683) |
Spastic paraplegia type 2 | (Orphanet:99015) |
Syringomyelia | (Orphanet:3280) |
X-linked spastic paraplegia type 16 | (Orphanet:100997) |
[DEL] SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE | (OMIM:607259) |