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Ontology Browser

Term:
Posterior Column Ataxia (DOID:9008995)
Annotations: Rat: (0) Mouse: (0) Human: (0) Chinchilla: (0) Bonobo: (0) Dog: (0) Squirrel: (0) Pig: (0)
Parent Terms Term With Siblings Child Terms
autosomal recessive spinocerebellar ataxia 19  
autosomal recessive spinocerebellar ataxia 2  
Cerebellar Atrophy with Seizures and Variable Developmental Delay  
CEREBELLAR ATROPHY, DEVELOPMENTAL DELAY, AND SEIZURES  
Cerebellar Atrophy, Visual Impairment, and Psychomotor Retardation  
Corneal Cerebellar Syndrome 
Dizziness +   
Friedreich ataxia +   
Galloway-Mowat syndrome +   
Growth Failure, Microcephaly, Mental Retardation, Cataracts, Large Joint Contractures, Osteoporosis, Cortical Dysplasia, and Cerebellar Atrophy 
Hearing Disorders +   
Hereditary Spinal Ataxia 
infantile cerebellar-retinal degeneration  
Mousa Al din Al Nassar Syndrome 
myoclonic cerebellar dyssynergia +  
NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR ATROPHY AND WITH OR WITHOUT SEIZURES  
Olfaction Disorders +   
olivopontocerebellar atrophy +   
Posterior Column Ataxia 
Somatosensory Disorders +   
Spinocerebellar Ataxias +   
Taste Disorders +   
Vision Disorders +   

Synonyms
Exact Synonyms: Biemond ataxia
Primary IDs: MESH:C536342 ;   RDO:0001888

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