Ontology Browser

Term:
Autosomal Recessive Spinocerebellar Ataxia 22 (DOID:9008970)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1)
Parent Terms Term With Siblings Child Terms
ataxia telangiectasia +   
ataxia with oculomotor apraxia type 1  
ataxia with oculomotor apraxia type 2  
ataxia with oculomotor apraxia type 3  
autosomal recessive spinocerebellar ataxia 10  
autosomal recessive spinocerebellar ataxia 11  
autosomal recessive spinocerebellar ataxia 12  
autosomal recessive spinocerebellar ataxia 13  
autosomal recessive spinocerebellar ataxia 14  
autosomal recessive spinocerebellar ataxia 15  
autosomal recessive spinocerebellar ataxia 16  
autosomal recessive spinocerebellar ataxia 17  
autosomal recessive spinocerebellar ataxia 18  
autosomal recessive spinocerebellar ataxia 19  
autosomal recessive spinocerebellar ataxia 2  
autosomal recessive spinocerebellar ataxia 20  
autosomal recessive spinocerebellar ataxia 21  
Autosomal Recessive Spinocerebellar Ataxia 22  
autosomal recessive spinocerebellar ataxia 25  
autosomal recessive spinocerebellar ataxia 26  
Autosomal Recessive Spinocerebellar Ataxia 6 
autosomal recessive spinocerebellar ataxia 7  
Autosomal Recessive Spinocerebellar Ataxia 8  
Autosomal Recessive Spinocerebellar Ataxia with Axonal Neuropathy +   
cerebellar ataxia, mental retardation and dysequlibrium syndrome +   
Charlevoix-Saguenay spastic ataxia  
Friedreich ataxia +   
mitochondrial DNA depletion syndrome 7  
primary coenzyme Q10 deficiency 4  

Synonyms
Exact Synonyms: SCAR22 ;   Spinocerebellar Ataxia 22
Primary IDs: MESH:C542540
Alternate IDs: OMIM:616948 ;   RDO:0004616 ;   RDO:9001203

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