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Ontology Browser
Term:
Branchial Myoclonus with Spastic Paraparesis and Cerebellar Ataxia (DOID:9001901)
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
cerebellar ataxia +     
Myoclonus +     
Spastic Paraparesis +     
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  
CATARACTS, SPASTIC PARAPARESIS, AND SPEECH DELAY  
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 Convulsive Disorder with Prenatal or Early Onset 
familial hemiplegic migraine 1  
Familial Myoclonus 1  
Familial Myoclonus 2  
Feigenbaum Bergeron Richardson Syndrome 
Furukawa Takagi Nakao Syndrome 
Gemignani 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  
Multiple Exostoses with Spastic Tetraparesis 
Myelocerebellar Disorder  
Myoclonic Epilepsies +   
Myoclonic Nystagmus 
Myoclonus, Cerebellar Ataxia, and Deafness 
Neonatal Intractable Myoclonus  
Neuhauser Eichner Opitz Syndrome 
NEURODEGENERATION, CHILDHOOD-ONSET, WITH CEREBELLAR ATAXIA AND COGNITIVE DECLINE  
Opsoclonus-Myoclonus Syndrome +   
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  
Spastic Paresis, Glaucoma, and Mental Retardation 
tropical spastic paraparesis  

Synonyms
Primary IDs: MESH:C566188
Alternate IDs: MIM:113610

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