Limb ataxia
Symptom Information:
Symptom ID: | HPO:0002070 | |||
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) Abnormality of coordination(HPO:0011443) Ataxia(HPO:0001251) Limb ataxia(HPO:0002070) MedDRA: |
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Database Frequency: | 41 / 7739 | |||
Resource: |
All diseases associated with this symptom:
Adult-onset autosomal recessive cerebellar ataxia | (Orphanet:284289) |
Alpha-mannosidosis | (Orphanet:61) |
Ataxia - oculomotor apraxia type 1 | (Orphanet:1168) |
Autosomal recessive ataxia, Beauce type | (Orphanet:88644) |
Autosomal recessive cerebellar ataxia - epilepsy - intellectual deficit | (Orphanet:284282) |
Autosomal recessive cerebellar ataxia - psychomotor retardation | (Orphanet:284271) |
Autosomal recessive progressive external ophthalmoplegia | (Orphanet:254886) |
Autosomal recessive spastic paraplegia type 48 | (Orphanet:306511) |
Autosomal recessive spastic paraplegia type 7 | (Orphanet:99013) |
CEREBELLAR ATAXIA, NEUROPATHY, AND VESTIBULAR AREFLEXIA SYNDROME | (OMIM:614575) |
Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia | (Orphanet:284324) |
Cystinuria | (Orphanet:214) |
Cystinuria type B | (Orphanet:93613) |
Friedreich ataxia | (Orphanet:95) |
Friedreich ataxia 1 | (OMIM:229300) |
Gerstmann-Straussler-Scheinker syndrome | (Orphanet:356) |
LEUKOENCEPHALOPATHY WITH ATAXIA | (OMIM:615651) |
LICHTENSTEIN-KNORR SYNDROME | (OMIM:616291) |
Marinesco-Sjögren syndrome | (Orphanet:559) |
SPINOCEREBELLAR ATAXIA 38 | (OMIM:615957) |
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 16 | (OMIM:615768) |
Spinocerebellar ataxia type 1 | (Orphanet:98755) |
Spinocerebellar ataxia type 10 | (Orphanet:98761) |
Spinocerebellar ataxia type 13 | (Orphanet:98768) |
Spinocerebellar ataxia type 15/16 | (Orphanet:98769) |
Spinocerebellar ataxia type 17 | (Orphanet:98759) |
Spinocerebellar ataxia type 19/22 | (Orphanet:98772) |
Spinocerebellar ataxia type 2 | (Orphanet:98756) |
Spinocerebellar ataxia type 20 | (Orphanet:101110) |
Spinocerebellar ataxia type 21 | (Orphanet:98773) |
Spinocerebellar ataxia type 23 | (Orphanet:101108) |
Spinocerebellar ataxia type 26 | (Orphanet:101112) |
Spinocerebellar ataxia type 27 | (Orphanet:98764) |
Spinocerebellar ataxia type 28 | (Orphanet:101109) |
Spinocerebellar ataxia type 29 | (Orphanet:208513) |
Spinocerebellar ataxia type 3 | (Orphanet:98757) |
Spinocerebellar ataxia type 31 | (Orphanet:217012) |
Spinocerebellar ataxia type 36 | (Orphanet:276198) |
Spinocerebellar ataxia type 5 | (Orphanet:98766) |
Spinocerebellar ataxia with axonal neuropathy type 2 | (Orphanet:64753) |
X-linked cerebral adrenoleukodystrophy | (Orphanet:139396) |