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Ontology Browser

Term:
Leber hereditary optic neuropathy with demyelinating disease of CNS (DOID:0111756)
Annotations: Rat: (0) Mouse: (0) Human: (0) Chinchilla: (0) Bonobo: (0) Dog: (0) Squirrel: (0) Pig: (0)
Parent Terms Term With Siblings Child Terms
Dysmyelinating Leukodystrophy with Oligodontia  
Dysmyelination with Jaundice 
early infantile epileptic encephalopathy 39  
hypomyelinating leukodystrophy +   
Hypomyelination with Brainstem and Spinal Cord Involvement and Leg Spasticity  
Krabbe disease +   
Leber hereditary optic neuropathy and dystonia  
Leber hereditary optic neuropathy with demyelinating disease of CNS 
A Leber plus disease characterized by Leber hereditary optic neuropathy and demyelination in the central nervous system. (DO)
megalencephalic leukoencephalopathy with subcortical cysts +   
Megalencephaly with Dysmyelination 
metachromatic leukodystrophy +   
Neurodevelopmental Disorder with Epilepsy, Cataracts, Feeding Difficulties, and Delayed Brain Myelination  
Neurodevelopmental Disorder with Microcephaly, Epilepsy, and Hypomyelination  
Optic Atrophy with Demyelinating Disease of CNS 
retinal vasculopathy with cerebral leukodystrophy  

Synonyms
Exact Synonyms: optic atrophy with demyelinating disease of CNS
Primary IDs: OMIM:165200
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/14213470 "DO"

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