epilepsy, idiopathic generalized, susceptibility to, 16
MONDO:0032827Mondo
Findings
No curated finding names epilepsy, idiopathic generalized, susceptibility to, 16 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal dominant inheritance
HPO, annotations 2026-09-02
Features
9 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.
- Global developmental delayHPOHP:0001263
- 2 of 2 reported patients
- Abnormal cerebral white matter morphologyHPOHP:0002500
- 1 of 2 reported patients
- Atypical absence seizureHPOHP:0007270
- 1 of 2 reported patients · Infantile onset
- MicrocephalyHPOHP:0000252
- 1 of 2 reported patients
- Multifocal epileptiform dischargesHPOHP:0010841
- 1 of 2 reported patients
- Myoclonic absence seizureHPOHP:0011150
- 1 of 2 reported patients · Childhood onset
- Myoclonic seizureHPOHP:0032794
- 1 of 2 reported patients
- Short statureHPOHP:0004322
- 1 of 2 reported patients
- Paroxysmal dyskinesiaHPOHP:0007166
- 0 of 2 reported patients
Where it sits
- A kind of
Other names
1 name
Resolves to: epilepsy, idiopathic generalized, susceptibility to, 16
- Also called
- EIG16