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Ontology Browser
Term:
Tremor of Intention, Ataxia, and Lipofuscinosis (DOID:9002945)
Annotations: Rat: (0) Mouse: (0) Human: (0) Chinchilla: (0) Bonobo: (0) Dog: (0) Squirrel: (0) Pig: (0) Naked Mole-rat: (0) Green Monkey: (0)
Parent Terms Term With Siblings Child Terms
Ataxia +     
lipid storage disease +     
Tremor +     
Abetalipoproteinemia Neuropathy  
adult-onset ataxia and polyneuropathy  
Arts syndrome  
Ataxia with Fasciculations 
Ataxia with Myoclonic Epilepsy and Presenile Dementia 
Ataxia, Deafness, and Cardiomyopathy 
ATAXIA, INTENTION TREMOR, AND HYPOTONIA SYNDROME, CHILDHOOD-ONSET  
ATAXIA, PROGRESSIVE SEIZURES, MENTAL DETERIORATION, AND HEARING LOSS  
Ataxia-Microcephaly-Cataract Syndrome 
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 
Cephalin Lipidosis 
Cerebroretinal Microangiopathy with Calcifications and Cysts +   
Chanarin-Dorfman syndrome +   
Childhood-onset Neurodegeneration with Ataxia, Tremor, Optic Atrophy, and Cognitive Decline  
Christianson syndrome  
COACH syndrome +   
coenzyme Q10 deficiency disease +   
congenital myopathy 16  
Deafness Hyperuricemia Neurologic Ataxia 
Diaminopentanuria 
essential tremor +   
Familial Cardiac Lipidosis 
familial isolated deficiency of vitamin E  
Farber lipogranulomatosis  
fragile X-associated tremor/ataxia syndrome  
Gait Ataxia +   
Geniospasm 
Global Developmental Delay, Progressive Ataxia, and Elevated Glutamine  
hereditary ataxia +   
hypomyelinating leukodystrophy 7  
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  
lysosomal acid lipase deficiency +   
Mitochondrial Myopathy, and Ataxia  
mucolipidosis +   
Muscular Atrophy, Ataxia, Retinitis Pigmentosa, and Diabetes Mellitus 
Myokymia 1  
Neurodegeneration with Ataxia and Late-Onset Optic Atrophy  
NEURODEVELOPMENTAL DISORDER WITH ATAXIA, HYPOTONIA, AND MICROCEPHALY  
neurodevelopmental disorder with eye movement abnormalities and ataxia  
Neurodevelopmental Disorder with Impaired Intellectual Development, Hypotonia, and Ataxia   
NEURODEVELOPMENTAL DISORDER WITH IMPAIRED LANGUAGE AND ATAXIA AND WITH OR WITHOUT SEIZURES  
NEURODEVELOPMENTAL DISORDER WITH INTENTION TREMOR, PYRAMIDAL SIGNS, DYSPRAXIA, AND OCULAR ANOMALIES  
neuronal ceroid lipofuscinosis +   
Neurovisceral Storage Disease with Curvilinear Bodies 
optic atrophy 10  
OPTIC ATROPHY-ATAXIA-PERIPHERAL NEUROPATHY-GLOBAL DEVELOPMENTAL DELAY SYNDROME  
Partington syndrome  
Peripheral Neuropathy, Ataxia, Focal Necrotizing Encephalopathy, and Spongy Degeneration of Brain 
PHARC syndrome  
Phospholipidosis  
Posterior Column Ataxia with Retinitis Pigmentosa  
Primary Orthostatic Tremor 
progressive myoclonus epilepsy 1B  
Reardon Wilson Cavanagh Syndrome 
Richards-Rundle Syndrome 
Sensory Ataxia, Autosomal Dominant 
Siddiqi syndrome  
Sjogren-Larsson syndrome +   
Spastic Paraplegia, Ataxia, and Mental Retardation 
sphingolipidosis +   
Spinocerebellar Ataxias +   
spondyloepimetaphyseal dysplasia, Genevieve-type  
steatotic liver disease +   
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 
xanthomatosis +   

Synonyms
Primary IDs: MESH:C566038
Alternate IDs: OMIM:190200

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