encephalitis/encephalopathy, mild, with reversible myelin vacuolization
MONDO:0020853Mondo
Findings
No curated finding names encephalitis/encephalopathy, mild, with reversible myelin vacuolization yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal dominant inheritance
- Onset and course
- Juvenile onset · Childhood onset
HPO, annotations 2026-09-02
Features
2 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Acute encephalopathyHPOHP:0006846
- 9 of 9 reported patients
- SeizureHPOHP:0001250
- 9 of 9 reported patients
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- MYRFHGNC:1181
- Limited · Ambry Genetics · Autosomal dominant · 2018
- Limited · Labcorp Genetics (formerly Invitae) · Unknown · 2018
Where it sits
- A kind of
Other names
2 names
Resolves to: encephalitis/encephalopathy, mild, with reversible myelin vacuolization
- Also called
- Encephalitis/encephalopathy, mild, with reversible splenial lesionMMERV