Truncal ataxia
Symptom Information:
Symptom ID: | HPO:0002078 | ||||
Synonyms: |
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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) Truncal ataxia(HPO:0002078) MedDRA: |
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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) |