narcolepsy 7
MONDO:0013652Mondo
Findings
No curated finding names narcolepsy 7 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Any narcolepsy in which the cause of the disease is a mutation in the MOG gene.
Definition from the Mondo Disease Ontology (MONDO:0013652), read 2026-09-29. CC BY 4.0.
- Inheritance
- Autosomal dominant inheritance
- Onset and course
- Young adult onset
HPO, annotations 2026-09-02
Features
7 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.
- CataplexyHPOHP:0002524
- 6 of 6 reported patients · Young adult onset
- Excessive daytime somnolenceHPOHP:0001262
- 6 of 6 reported patients · Young adult onset
- ObesityHPOHP:0001513
- 5 of 6 reported patients
- Hypnagogic hallucinationHPOHP:0002519
- 3 of 6 reported patients
- Obstructive sleep apneaHPOHP:0002870
- 3 of 6 reported patients
- Sleep paralysisHPOHP:0025233
- 3 of 6 reported patients
- Type II diabetes mellitus
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.
- MOGHGNC:7197
- Limited · Labcorp Genetics (formerly Invitae) · Unknown · 2017
- Limited · PanelApp Australia · Autosomal dominant · 2025
Where it sits
Other names
3 names
Resolves to: narcolepsy 7
- Also called
- MOG narcolepsynarcolepsy caused by mutation in MOGnarcolepsy type 7