Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
Ataxia +     
Abetalipoproteinemia 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 
CANOMAD Syndrome 
Carnitine Acetyltransferase Deficiency  
Cataract Ataxia Deafness 
Cataracts, Ataxia, Short Stature, and Mental Retardation 
Cerebroretinal Microangiopathy with Calcifications and Cysts +   
Christianson syndrome  
COACH Syndrome  
coenzyme Q10 deficiency disease +   
Deafness Hyperuricemia Neurologic Ataxia 
Diaminopentanuria 
Erythrokeratodermia with Ataxia  
familial isolated deficiency of vitamin E  
gait apraxia 
Gait Ataxia  
Impairment of the ability to coordinate the movements required for normal ambulation (WALKING) which may result from impairments of motor function or sensory feedback. This condition may be associated with BRAIN DISEASES (including CEREBELLAR DISEASES and BASAL GANGLIA DISEASES); SPINAL CORD DISEASES; or PERIPHERAL NERVOUS SYSTEM DISEASES.
hereditary 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 
Joubert syndrome 7  
Leukoencephalopathy with Ataxia  
Mitochondrial Myopathy, and Ataxia  
Muscular Atrophy, Ataxia, Retinitis Pigmentosa, and Diabetes Mellitus 
Myokymia 1  
NEURODEGENERATION, CHILDHOOD-ONSET, STRESS-INDUCED, WITH VARIABLE ATAXIA AND SEIZURES  
Neurodevelopmental Disorder with Impaired Intellectual Development, Hypotonia, and Ataxia   
Optic Atrophy 10 with or without Ataxia, Mental Retardation, and Seizures  
Partington syndrome  
Peripheral Neuropathy, Ataxia, Focal Necrotizing Encephalopathy, and Spongy Degeneration of Brain 
PHARC syndrome  
Posterior Column Ataxia with Retinitis Pigmentosa  
Reardon Wilson Cavanagh Syndrome 
Richards-Rundle Syndrome 
Sensory Ataxia, Autosomal Dominant  
Spastic Ataxia with Congenital Miosis 
Spastic Paraplegia, Ataxia, and Mental Retardation 
Spinocerebellar Ataxias +   
Spondyloepimetaphyseal Dysplasia, Genevieve Type  
Tapetoretinal Degeneration with Ataxia 
Treft Sanborn Carey Syndrome 
Tremor of Intention, Ataxia, and Lipofuscinosis 
Tryptophanuria with Dwarfism 

Synonyms
Exact Synonyms: Ataxia of Gait ;   Cerebellar Gait ;   Cerebellar Gait Ataxia ;   Cerebellar Gait Ataxias ;   Cerebellar Gaits ;   Gait Ataxias ;   Sensory Gait Ataxia ;   Sensory Gait Ataxias
Primary IDs: MESH:D020234
Alternate IDs: RDO:0007366
Definition Sources: MESH:D020234

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