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Online Mendelian Inheritance in Man
Last uploaded:
March 22, 2026
| Id | http://purl.bioontology.org/ontology/OMIM/618113
http://purl.bioontology.org/ontology/OMIM/618113
|
|---|---|
| Preferred Name | ENCEPHALITIS/ENCEPHALOPATHY, MILD, WITH REVERSIBLE MYELIN VACUOLIZATION |
| Synonyms |
MERS
ENCEPHALITIS/ENCEPHALOPATHY, MILD, WITH REVERSIBLE SPLENIAL LESION
MMERV
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| altLabel |
MERS
ENCEPHALITIS/ENCEPHALOPATHY, MILD, WITH REVERSIBLE SPLENIAL LESION
MMERV
|
|---|---|
| prefLabel | ENCEPHALITIS/ENCEPHALOPATHY, MILD, WITH REVERSIBLE MYELIN VACUOLIZATION
|
| Gene Symbol |
NNO1
C11orf9
KIAA0954
CUGS
MMERV
MYRF
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| Scope Statement | No permanent neurologic sequelae [MISCELLANEOUS]
Two unrelated Japanese families have been reported (last curated September 2018) [MISCELLANEOUS]
Brain imaging abnormalities are transient and return to normal [MISCELLANEOUS]
Affected individuals have complete neurologic recovery within days to weeks [MISCELLANEOUS]
Caused by mutation in the myelin regulatory factor gene (MYRF, 608329.0001) [MOLECULAR BASIS]
Episodes may be triggered by fever, infection, stress [MISCELLANEOUS]
Onset in childhood [MISCELLANEOUS]
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| type | |
| Has manifestation |
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| tui | T047
|
| Gene Locus | 11q12.2
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| MIMTYPEMEANING | Phenotype description, molecular basis known.
|
| notation | 618113
|
| Semantic type UMLS property | |
| Has inheritance type | |
| cui | C4722446
|
| OMIM Entry Type | 3
|
| OMIM MimType Value | pound
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| Delete | Subject | Author | Type | Created |
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| No notes to display |