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Ontology Browser

Term:
CEREBELLAR ATAXIA INFANTILE WITH PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA (DOID:9003108)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
3-methylglutaconic aciduria type 5  
ataxia with oculomotor apraxia type 1  
autosomal dominant cerebellar ataxia +   
autosomal dominant progressive external ophthalmoplegia 1  
autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2  
autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3  
autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 4  
autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 5  
autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 6  
autosomal recessive cerebellar ataxia +   
Benign Cerebellar Ataxia with Thermoanalgesia 
Brachydactyly-Nystagmus-Cerebellar Ataxia 
Branchial Myoclonus with Spastic Paraparesis and Cerebellar Ataxia 
CAPOS Syndrome  
Cayman type cerebellar ataxia  
Cerebellar Ataxia and Hypergonadotropic Hypogonadism 
Cerebellar Ataxia and Hypogonadotropic Hypogonadism  
Cerebellar Ataxia and Neurosensory Deafness 
Cerebellar Ataxia Ectodermal Dysplasia 
CEREBELLAR ATAXIA INFANTILE WITH PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA  
CEREBELLAR ATAXIA, NEUROPATHY, AND VESTIBULAR AREFLEXIA SYNDROME  
Cerebellar Hypoplasia with Endosteal Sclerosis  
Cerebellofaciodental Syndrome  
Cerebelloparenchymal Disorder II 
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  
Familial Horizontal Gaze Palsy with Progressive Scoliosis +   
Furukawa Takagi Nakao Syndrome 
Gillespie Syndrome  
Harding Ataxia 
Herrmann Syndrome 
ITM2B-related cerebral amyloid angiopathy 2  
Kearns-Sayre syndrome  
Laryngeal Abductor Paralysis with Cerebellar Ataxia and Motor Neuropathy 
Marinesco-Sjogren syndrome  
Myelocerebellar Disorder  
Myoclonus, Cerebellar Ataxia, and Deafness 
Neuhauser Eichner Opitz Syndrome 
nonprogressive cerebellar ataxia with mental retardation  
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Recessive +   
Progressive External Ophthalmoplegia with Myoclonus  
Renal Tubulopathy, Diabetes Mellitus, and Cerebellar Ataxia due to Duplication of Mitochondrial DNA 
short-rib thoracic dysplasia 9 with or without polydactyly  

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