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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
hereditary ataxia +     
autosomal dominant sensory ataxia 1  
Boucher-Neuhauser syndrome  
cerebellar ataxia +   
A hereditary ataxia that is characterized by ataxia originating in the cerebellum. (DO)
episodic ataxia +   
Gemignani Syndrome 
INTELLECTUAL DEVELOPMENTAL DISORDER WITH POOR GROWTH AND WITH OR WITHOUT SEIZURES OR ATAXIA  
MITOCHONDRIAL DNA DEPLETION SYNDROME 16B  
spastic ataxia +   
Spinocerebellar Ataxia and Plaque-Like Deposits  
Spinocerebellar Ataxia with Dysmorphism 
Spinocerebellar Ataxia with Epilepsy  
Spinocerebellar Ataxia with Rigidity and Peripheral Neuropathy 
X-linked hereditary ataxia +   
X-linked sideroblastic anemia with ataxia  
X-linked spinocerebellar ataxia 1  
X-linked spinocerebellar ataxia 2 
X-linked spinocerebellar ataxia 3 
X-linked spinocerebellar ataxia 4 
X-linked spinocerebellar ataxia 5 

Synonyms
Exact Synonyms: Adiadochokinesis ;   Cerebellar Dysmetria ;   Cerebellar Dysmetrias ;   Cerebellar Hemiataxia ;   Cerebellar Hemiataxias ;   Cerebellar Incoordination ;   Cerebellar Incoordinations ;   Dysmetria ;   Dysmetrias ;   adiadochokineses ;   cerebellar ataxias ;   hypermetria ;   hypermetrias
Narrow Synonyms: Ataxia, cerebellar, juvenile to adolescent, RAB24-related ;   Ataxia, cerebellar, neonatal ;   Ataxia, cerebellar, neonatal, GRM1-related ;   Ataxia, cerebellar, progressive early-onset ;   Ataxia, cerebellar, progressive early-onset, SEL1L-related ;   cerebellar ataxia, juvenile to adolescent ;   neurodegenerative vacuolar storage disease
Primary IDs: MESH:D002524
Alternate IDs: OMIA:000078 ;   OMIA:001692 ;   OMIA:001913 ;   OMIA:001954 ;   OMIA:002110
Definition Sources: http://en.wikipedia.org/wiki/Cerebellar_ataxia "DO" "DO"

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