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Ontology Browser

Term:
X-linked spinocerebellar ataxia 3 (DOID:0111831)
Annotations: Rat: (0) Mouse: (0) Human: (0) Chinchilla: (0) Bonobo: (0) Dog: (0) Squirrel: (0) Pig: (0)
Parent Terms Term With Siblings Child Terms
Boucher-Neuhauser syndrome  
cerebellar ataxia +   
Gemignani Syndrome 
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 sideroblastic anemia with ataxia  
X-linked spinocerebellar ataxia 1  
X-linked spinocerebellar ataxia 2 
X-linked spinocerebellar ataxia 3 
An X-linked cerebellar ataxia characterized by onset in infancy of hypotonia, ataxia, sensorineural deafness, developmental delay, esotropia, and optic atrophy with X-linked inheritance. (DO)
X-linked spinocerebellar ataxia 4 
X-linked spinocerebellar ataxia 5 

Synonyms
Exact Synonyms: SCAX3 ;   Schmidley syndrome ;   X-linked ataxia-deafness syndrome ;   X-linked spinocerebellar ataxia type 3
Primary IDs: MESH:C537315
Alternate IDs: OMIM:301790
Xrefs: GARD:9981 ;   ORDO:85297
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/3614654 "DO"

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