Limb ataxia

Symptom Information:

Symptom ID: HPO:0002070
Synonyms:
Appendicular ataxia [HPO:0002070]
Appendicular ataxia [OMIM:Appendicular ataxia]
Limb ataxia [OMIM:Limb ataxia]
Quality:
Cross references:
OMIM: "Appendicular ataxia" [OMIM:Appendicular ataxia]
OMIM: "Limb ataxia" [OMIM:Limb ataxia]
Is a (Direct Parents):
HPO         Ataxia
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:
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)