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Ontology Browser

Optic Atrophy with Demyelinating Disease of CNS (DOID:9000004)
Annotations: Rat: (0) Mouse: (0) Human: (0) Chinchilla: (0) Bonobo: (0) Dog: (0) Squirrel: (0) Pig: (0)
Parent Terms Term With Siblings Child Terms
Berk-Tabatznik Syndrome 
Bosch-Boonstra-Schaaf Optic Atrophy Syndrome  
Charcot-Marie-Tooth disease X-linked recessive 5  
dominant optic atrophy plus syndrome  
Dysmyelinating Leukodystrophy with Oligodontia  
Dysmyelination with Jaundice 
early infantile epileptic encephalopathy 39  
Friedreich Ataxia, So-Called, with Optic Atrophy and Sensorineural Deafness 
Growth Retardation, Alopecia, Pseudoanodontia and Optic Atrophy  
Hagemoser Weinstein Bresnick Syndrome 
hypomyelinating leukodystrophy +   
Hypomyelination with Brainstem and Spinal Cord Involvement and Leg Spasticity  
Konigsmark Knox Hussels Syndrome 
Krabbe disease +   
Leber hereditary optic neuropathy +   
Leber hereditary optic neuropathy with demyelinating disease of CNS 
megalencephalic leukoencephalopathy with subcortical cysts +   
Megalencephaly with Dysmyelination 
metachromatic leukodystrophy +   
Metaphyseal Dysplasia, Anetoderma, and Optic Atrophy 
Neurodevelopmental Disorder with Epilepsy, Cataracts, Feeding Difficulties, and Delayed Brain Myelination  
Neurodevelopmental Disorder with Microcephaly, Epilepsy, and Hypomyelination  
optic atrophy 1  
optic atrophy 10  
optic atrophy 11  
Optic Atrophy 12  
Optic Atrophy 13 
optic atrophy 2 
optic atrophy 3  
optic atrophy 4 
optic atrophy 5  
optic atrophy 6 
optic atrophy 7  
optic atrophy 8 
optic atrophy 9  
Optic Atrophy Spastic Paraplegia Syndrome 
Optic Atrophy with Demyelinating Disease of CNS 
Optic Atrophy, Deafness, Ophthalmoplegia, and Myopathy 
Progressive Encephalopathy with Amyotrophy and Optic Atrophy  
retinal vasculopathy with cerebral leukodystrophy  
Senior-Loken syndrome +   
Spastic Paraplegia, Optic Atrophy, and Dementia 
Spastic Paraplegia, Optic Atrophy, Microcephaly, and XY Sex Reversal 
Subacute Necrotizing Encephalomyelopathy of Leigh, Adult 
Wolfram syndrome +   

Primary IDs: MESH:C563496 ;   RDO:0012738

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