Truncal ataxia

Symptom Information:

Symptom ID: HPO:0002078
Synonyms:
Trunk ataxia [HPO:0002078]
Truncal ataxia [OMIM:Truncal ataxia]
Trunk ataxia [OMIM:Trunk ataxia]
Ataxia, truncal [OMIM:Ataxia, truncal]
Quality:
Cross references:
OMIM: "Truncal ataxia" [OMIM:Truncal ataxia]
OMIM: "Trunk ataxia" [OMIM:Trunk ataxia]
OMIM: "Ataxia, truncal" [OMIM:Ataxia, truncal]
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)
                      Truncal ataxia(HPO:0002078)
MedDRA:
Database Frequency: 41 / 7739
Resource:

All diseases associated with this symptom:

Adult-onset autosomal recessive cerebellar ataxia (Orphanet:284289)
Ataxia - oculomotor apraxia type 1 (Orphanet:1168)
Autosomal recessive cerebellar ataxia - psychomotor retardation (Orphanet:284271)
Autosomal recessive spastic paraplegia type 7 (Orphanet:99013)
BRANCHIAL MYOCLONUS WITH SPASTIC PARAPARESIS AND CEREBELLAR ATAXIA (OMIM:113610)
Bilateral frontoparietal polymicrogyria (Orphanet:101070)
CADASIL (Orphanet:136)
CEREBELLAR ATAXIA, AREFLEXIA, PES CAVUS, OPTIC ATROPHY, AND SENSORINEURALHEARING LOSS (OMIM:601338)
CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME1 (OMIM:224050)
CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME2 (OMIM:610185)
CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME4 (OMIM:615268)
COG5-CDG (Orphanet:263487)
Christianson syndrome (Orphanet:85278)
Cystinuria (Orphanet:214)
Cystinuria type B (Orphanet:93613)
Dandy-Walker malformation - postaxial polydactyly (Orphanet:1566)
Dysequilibrium syndrome (Orphanet:1766)
ENCEPHALOPATHY, RECURRENT, OF CHILDHOOD (OMIM:130950)
Episodic ataxia type 6 (Orphanet:209967)
Facial dysmorphism - macrocephaly - myopia - Dandy-Walker malformation (Orphanet:1970)
Friedreich ataxia 1 (OMIM:229300)
Gerstmann-Straussler-Scheinker syndrome (Orphanet:356)
Isolated Dandy-Walker malformation (Orphanet:217)
Microcephaly-cerebellar hypoplasia-cardiac conduction defect syndrome (Orphanet:329332)
N-ACETYLASPARTATE DEFICIENCY (OMIM:614063)
Progressive myoclonic epilepsy type 3 (Orphanet:263516)
Rett syndrome (Orphanet:778)
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 16 (OMIM:615768)
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 17 (OMIM:616127)
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 18 (OMIM:616204)
Spastic ataxia with congenital miosis (Orphanet:1182)
Spinocerebellar ataxia type 1 (Orphanet:98755)
Spinocerebellar ataxia type 15/16 (Orphanet:98769)
Spinocerebellar ataxia type 19/22 (Orphanet:98772)
Spinocerebellar ataxia type 26 (Orphanet:101112)
Spinocerebellar ataxia type 27 (Orphanet:98764)
Spinocerebellar ataxia type 3 (Orphanet:98757)
USHER SYNDROME, TYPE IIIB (OMIM:614504)
Wiedemann-Rautenstrauch syndrome (Orphanet:3455)
Wolfram syndrome 1 (OMIM:222300)
X-linked cerebral adrenoleukodystrophy (Orphanet:139396)