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Ontology Browser
Term:
cerebellar ataxia
(DOID:0050753)
Annotations:
Rat: (482)
Mouse: (501)
Human: (672)
Chinchilla: (451)
Bonobo: (476)
Dog: (484)
Squirrel: (454)
Pig: (473)
Naked Mole-rat: (452)
Green Monkey: (473)
Parent Terms
Term With Siblings
Child Terms
hereditary ataxia
+
Spinocerebellar Ataxias
+
autosomal dominant sensory ataxia 1
Boucher-Neuhauser syndrome
cerebellar ataxia
+
A hereditary ataxia that is characterized by ataxia originating in the cerebellum. (DO)
episodic ataxia
+
Gemignani Syndrome
INTELLECTUAL DEVELOPMENTAL DISORDER WITH POOR GROWTH AND WITH OR WITHOUT SEIZURES OR ATAXIA
mitochondrial DNA depletion syndrome 16B
spastic ataxia
+
Spinocerebellar Ataxia and Plaque-Like Deposits
Spinocerebellar Ataxia with Dysmorphism
Spinocerebellar Ataxia with Epilepsy
Spinocerebellar Ataxia with Rigidity and Peripheral Neuropathy
X-linked hereditary ataxia
+
X-linked sideroblastic anemia with ataxia
X-linked spinocerebellar ataxia 1
X-linked spinocerebellar ataxia 2
X-linked spinocerebellar ataxia 3
X-linked spinocerebellar ataxia 4
X-linked spinocerebellar ataxia 5
3-methylglutaconic aciduria type 5
autosomal dominant cerebellar ataxia
+
autosomal recessive cerebellar ataxia
+
Benign Cerebellar Ataxia with Thermoanalgesia
Brachydactyly-Nystagmus-Cerebellar Ataxia
Branchial Myoclonus with Spastic Paraparesis and Cerebellar Ataxia
CAPOS Syndrome
Cerebellar Ataxia and Ectodermal Dysplasia
Cerebellar Ataxia and Hypergonadotropic Hypogonadism
Cerebellar Ataxia and Neurosensory Deafness
CEREBELLAR ATAXIA INFANTILE WITH PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA
CEREBELLAR ATAXIA, BRAIN ABNORMALITIES, AND CARDIAC CONDUCTION DEFECTS
Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome
cerebellofaciodental syndrome
Combined Cerebellar and Peripheral Ataxia with Hearing Loss and Diabetes Mellitus
CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND CEREBELLAR ATAXIA
episodic ataxia type 5
episodic ataxia type 6
familial hemiplegic migraine 1
Furukawa Takagi Nakao Syndrome
Gillespie syndrome
Gordon Holmes syndrome
Harding Ataxia
Herrmann Syndrome
hypomyelinating leukodystrophy 8
ITM2B-related cerebral amyloid angiopathy 2
Laryngeal Abductor Paralysis with Cerebellar Ataxia and Motor Neuropathy
Mitochondrial Myopathy, and Ataxia
Myelocerebellar Disorder
Myoclonus, Cerebellar Ataxia, and Deafness
Neuhauser Eichner Opitz Syndrome
NEURODEGENERATION, CHILDHOOD-ONSET, WITH CEREBELLAR ATAXIA AND COGNITIVE DECLINE
Renal Tubulopathy, Diabetes Mellitus, and Cerebellar Ataxia due to Duplication of Mitochondrial DNA
short-rib thoracic dysplasia 9 with or without polydactyly
Synonyms
Exact Synonyms:
Adiadochokinesis ; Cerebellar Dysmetria ; Cerebellar Dysmetrias ; Cerebellar Hemiataxia ; Cerebellar Hemiataxias ; Cerebellar Incoordination ; Cerebellar Incoordinations ; Dysmetria ; Dysmetrias ; adiadochokineses
Narrow Synonyms:
Ataxia, cerebellar, juvenile to adolescent, RAB24-related ; Ataxia, cerebellar, neonatal ; Ataxia, cerebellar, neonatal, GRM1-related ; Ataxia, cerebellar, progressive early-onset ; Ataxia, cerebellar, progressive early-onset, SEL1L-related ; cerebellar ataxia, juvenile to adolescent ; neurodegenerative vacuolar storage disease
Primary IDs:
MESH:D002524
Alternate IDs:
OMIA:000078 ; OMIA:001692 ; OMIA:001913 ; OMIA:001954 ; OMIA:002110
Definition Sources:
http://en.wikipedia.org/wiki/Cerebellar_ataxia
"DO" "DO"