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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
Ataxia +     
Abetalipoproteinemia Neuropathy  
adult-onset ataxia and polyneuropathy  
Arts syndrome  
Ataxia with Fasciculations 
Ataxia with Myoclonic Epilepsy and Presenile Dementia 
Ataxia, Deafness, and Cardiomyopathy 
ATAXIA, PROGRESSIVE SEIZURES, MENTAL DETERIORATION, AND HEARING LOSS  
Ataxia-Microcephaly-Cataract Syndrome 
Ataxia-Oculomotor Apraxia 4  
ataxic cerebral palsy 
Atonic-Astatic Syndrome of Foerster 
autosomal recessive spinocerebellar ataxia 19  
autosomal recessive spinocerebellar ataxia 2  
Bangstad Syndrome 
Behr syndrome  
Benign Childhood Paroxysmal Tonic Upgaze with Ataxia 
Bhaskar Jagannathan Syndrome 
CANOMAD Syndrome 
Carnitine Acetyltransferase Deficiency  
Cataract Ataxia Deafness 
Cataracts, Ataxia, Short Stature, and Mental Retardation 
Cerebellar Atrophy with Seizures and Variable Developmental Delay  
CEREBELLAR ATROPHY, DEVELOPMENTAL DELAY, AND SEIZURES  
Cerebellar Atrophy, Visual Impairment, and Psychomotor Retardation  
Cerebroretinal Microangiopathy with Calcifications and Cysts +   
Childhood-onset Neurodegeneration with Ataxia, Tremor, Optic Atrophy, and Cognitive Decline  
Christianson syndrome  
COACH syndrome  
coenzyme Q10 deficiency disease +   
Corneal Cerebellar Syndrome 
Deafness Hyperuricemia Neurologic Ataxia 
Diaminopentanuria 
Erythrokeratodermia with Ataxia 
familial isolated deficiency of vitamin E  
Friedreich ataxia +   
Gait Ataxia +   
Galloway-Mowat syndrome +   
Global Developmental Delay, Progressive Ataxia, and Elevated Glutamine  
Growth Failure, Microcephaly, Mental Retardation, Cataracts, Large Joint Contractures, Osteoporosis, Cortical Dysplasia, and Cerebellar Atrophy 
hereditary ataxia +   
Hereditary Spinal Ataxia 
hypomyelinating leukodystrophy 7 with or without oligodontia and-or hypogonadotropic hypogonadism  
HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME  
HYPOTONIA, ATAXIA, DEVELOPMENTAL DELAY, AND TOOTH ENAMEL DEFECT SYNDROME  
Hypotonia, Congenital Nystagmus, Ataxia and Abnormal Auditory Brainstem Response 
infantile cerebellar-retinal degeneration  
Joubert syndrome 7  
Leukoencephalopathy with Ataxia  
Mitochondrial Myopathy, and Ataxia  
Mousa Al din Al Nassar Syndrome 
Muscular Atrophy, Ataxia, Retinitis Pigmentosa, and Diabetes Mellitus 
myoclonic cerebellar dyssynergia +  
Myokymia 1  
NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR ATROPHY AND WITH OR WITHOUT SEIZURES  
Neurodevelopmental Disorder with Impaired Intellectual Development, Hypotonia, and Ataxia   
olivopontocerebellar atrophy +   
optic atrophy 10  
Partington syndrome  
Peripheral Neuropathy, Ataxia, Focal Necrotizing Encephalopathy, and Spongy Degeneration of Brain 
PHARC syndrome  
Posterior Column Ataxia 
Posterior Column Ataxia with Retinitis Pigmentosa  
progressive myoclonus epilepsy 1B  
Reardon Wilson Cavanagh Syndrome 
Richards-Rundle Syndrome 
Sensory Ataxia, Autosomal Dominant  
Spastic Ataxia with Congenital Miosis 
Spastic Paraplegia, Ataxia, and Mental Retardation 
Spinocerebellar Ataxias +   
A group of dominantly inherited, predominately late-onset, cerebellar ataxias which have been divided into multiple subtypes based on clinical features and genetic mapping. Progressive ataxia is a central feature of these conditions, and in certain subtypes POLYNEUROPATHY; DYSARTHRIA; visual loss; and other disorders may develop. (From Joynt, Clinical Neurology, 1997, Ch65, pp 12-17; J Neuropathol Exp Neurol 1998 Jun;57(6):531-43)
spondyloepimetaphyseal dysplasia, Genevieve-type  
stress-induced childhood-onset neurodegeneration with variable ataxia and seizures  
Tapetoretinal Degeneration with Ataxia 
Treft Sanborn Carey Syndrome 
Tremor of Intention, Ataxia, and Lipofuscinosis 
Tryptophanuria with Dwarfism 

Synonyms
Exact Synonyms: cerebellar degeneration with slow eye movements ;   dominantly inherited spinocerebellar ataxias ;   dominantly-inherited spinocerebellar ataxia ;   spinocerebellar ataxia ;   spinocerebellar atrophies ;   spinocerebellar atrophy
Narrow Synonyms: SDSEM AMYOTROPHIC LATERAL SCLEROSIS, SUSCEPTIBILITY TO, 13 ;   SPINOCEREBELLAR ATAXIA, DOMINANT ;   spinocerebellar ataxia, recessive
Primary IDs: MESH:D020754
Definition Sources: MESH:D020754

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