developmental delay with or without epilepsy
MONDO:0957815Mondo
Findings
No curated finding names developmental delay with or without epilepsy 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
- Congenital onset · Infantile onset · Childhood onset
HPO, annotations 2026-09-02
Features
28 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.
- Focal-onset seizureHPOHP:0007359
- 1 of 1 reported patient
- SeizureHPOHP:0001250
- 1 of 1 reported patient
- Delayed speech and language developmentHPOHP:0000750
- 13 of 15 reported patients
- Intellectual disabilityHPOHP:0001249
- 15 of 20 reported patients
- Motor delayHPOHP:0001270
- 10 of 16 reported patients
- Autistic behaviorHPOHP:0000729
- 2 of 5 reported patients
- Cerebellar atrophyHPOHP:0001272
- 5 of 13 reported patients
- AtaxiaHPOHP:0001251
- 5 of 21 reported patients
- EEG with frontal focal spikesHPOHP:0012015
- 2 of 9 reported patients
- EEG with polyspike wave complexesHPOHP:0002392
- 2 of 9 reported patients
- Multifocal epileptiform dischargesHPOHP:0010841
- 2 of 9 reported patients
- MicrocephalyHPOHP:0000252
- 4 of 20 reported patients
Show the remaining 16
- Spastic gaitHPOHP:0002064
- 1 of 5 reported patients
- Febrile seizure (within the age range of 3 months to 6 years)HPOHP:0002373
- 4 of 21 reported patients
- Myoclonic seizureHPOHP:0032794
- 4 of 21 reported patients
- StrabismusHPOHP:0000486
- 3 of 16 reported patients
- Attention deficit hyperactivity disorderHPOHP:0007018
- 3 of 21 reported patients
- HypotoniaHPOHP:0001252
- 3 of 21 reported patients
Where it sits
- A kind of