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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 +   
Incoordination of voluntary movements that occur as a manifestation of CEREBELLAR DISEASES. Characteristic features include a tendency for limb movements to overshoot or undershoot a target (dysmetria), a tremor that occurs during attempted movements (intention TREMOR), impaired force and rhythm of diadochokinesis (rapidly alternating movements), and GAIT ATAXIA. (From Adams et al., Principles of Neurology, 6th ed, p90)
episodic ataxia +   
Gemignani Syndrome 
INTELLECTUAL DEVELOPMENTAL DISORDER WITH POOR GROWTH AND WITH OR WITHOUT SEIZURES OR ATAXIA  
Machado-Joseph disease  
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 Ataxias ;   Cerebellar Dysmetria ;   Cerebellar Dysmetrias ;   Cerebellar Hemiataxia ;   Cerebellar Hemiataxias ;   Cerebellar Incoordination ;   Cerebellar Incoordinations ;   Dysmetria ;   Dysmetrias ;   Hypermetria ;   adiadochokineses ;   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 ;   RDO:0000422
Definition Sources: http://en.wikipedia.org/wiki/Cerebellar_ataxia "DO", MESH:D002524

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.