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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
Ataxia +     
Abetalipoproteinemia Neuropathy 
aceruloplasminemia  
agenesis of the corpus callosum with peripheral neuropathy  
Arts syndrome  
Ataxia and Polyneuropathy, Adult-Onset  
Ataxia with Fasciculations 
Ataxia with Myoclonic Epilepsy and Presenile Dementia 
ataxia with oculomotor apraxia type 3  
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 
Bangstad Syndrome 
Behr Syndrome  
Benign Childhood Paroxysmal Tonic Upgaze with Ataxia 
Bhaskar Jagannathan Syndrome 
BRAIN ABNORMALITIES, NEURODEGENERATION, AND DYSOSTEOSCLEROSIS  
CANOMAD Syndrome 
Carnitine Acetyltransferase Deficiency  
Cataract Ataxia Deafness 
Cataracts, Ataxia, Short Stature, and Mental Retardation 
Cerebroretinal Microangiopathy with Calcifications and Cysts +   
Childhood-Onset Neurodegeneration with Ataxia, Dystonia, and Gaze Palsy  
Childhood-Onset Neurodegeneration with Brain Atrophy  
Childhood-Onset Neurodegeneration with Cerebellar Atrophy  
Christianson syndrome  
Chronic Traumatic Encephalopathy 
COACH Syndrome  
coenzyme Q10 deficiency disease +   
Deafness Hyperuricemia Neurologic Ataxia 
demyelinating disease +   
Diaminopentanuria 
Erythrokeratodermia with Ataxia  
eye degenerative disease +   
eyelid degenerative disease +  
familial isolated deficiency of vitamin E  
Feigenbaum Bergeron Richardson Syndrome 
FINCA Syndrome  
Gait Ataxia +   
Global Developmental Delay, Progressive Ataxia, and Elevated Glutamine  
hereditary ataxia +   
A neurodegenerative disease that is characterized by slowly progressive incoordination of gait and often associated with poor coordination of hands, speech, and eye movements. (DO)
Huntington's disease-like 2  
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 
Idiopathic Basal Ganglia Calcification 1  
Idiopathic Basal Ganglia Calcification 6  
Idiopathic Basal Ganglia Calcification 7  
infantile cerebellar-retinal degeneration  
Joubert syndrome 7  
Leukoencephalopathy with Ataxia  
Metabolic Crises, Recurrent, with Variable Encephalomyopathic Features and Neurologic Regression  
Mitochondrial Myopathy, and Ataxia  
motor neuron disease +   
multiple system atrophy +   
Muscular Atrophy, Ataxia, Retinitis Pigmentosa, and Diabetes Mellitus 
myoclonic cerebellar dyssynergia +  
Myokymia 1  
Nervous System Heredodegenerative Disorders +   
neurodegeneration with brain iron accumulation +   
NEURODEGENERATION, CHILDHOOD-ONSET, STRESS-INDUCED, WITH VARIABLE ATAXIA AND SEIZURES  
NEURODEGENERATION, EARLY-ONSET, WITH CHOREOATHETOID MOVEMENTS AND MICROCYTIC ANEMIA  
Neurodevelopmental Disorder with Impaired Intellectual Development, Hypotonia, and Ataxia   
Neuronal Intranuclear Inclusion Disease  
olivopontocerebellar atrophy +   
Optic Atrophy 10 with or without Ataxia, Mental Retardation, and Seizures  
Paraneoplastic Syndromes, Nervous System +   
Partington syndrome  
PEHO syndrome  
Peripheral Neuropathy, Ataxia, Focal Necrotizing Encephalopathy, and Spongy Degeneration of Brain 
PHARC syndrome  
Pick's disease  
plexopathy 
pontocerebellar hypoplasia +   
Posterior Column Ataxia with Retinitis Pigmentosa  
postpoliomyelitis syndrome 
primary cerebellar degeneration +   
prion disease +   
Radiation Sensitivity Chromosome Instability Syndrome, Autosomal Dominant 
Reardon Wilson Cavanagh Syndrome 
Richards-Rundle Syndrome 
secondary Parkinson disease +   
Sensory Ataxia, Autosomal Dominant  
Spastic Ataxia with Congenital Miosis 
Spastic Paraplegia, Ataxia, and Mental Retardation 
Spastic Pseudosclerosis 
Spinocerebellar Ataxias +   
spondyloepimetaphyseal dysplasia, Genevieve-type  
Subacute Combined Degeneration  
synucleinopathy +   
Tapetoretinal Degeneration with Ataxia 
tauopathy +   
TDP-43 Proteinopathies +   
Treft Sanborn Carey Syndrome 
Tremor of Intention, Ataxia, and Lipofuscinosis 
Tryptophanuria with Dwarfism 

Synonyms
Primary IDs: RDO:9004372
Xrefs: GARD:6614 ;   OMIM:PS164400
Definition Sources: http://www.ncbi.nlm.nih.gov/books/NBK1138

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