neurodevelopmental disorder with infantile epileptic spasms
MONDO:0859162Mondo
Findings
No curated finding names neurodevelopmental disorder with infantile epileptic spasms 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
- Infantile onset
HPO, annotations 2026-09-02
Features
12 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.
- Delayed ability to walkHPOHP:0031936
- 2 of 2 reported patients
- Delayed speech and language developmentHPOHP:0000750
- 2 of 2 reported patients
- Epileptic spasmHPOHP:0011097
- 2 of 2 reported patients
- Intellectual disabilityHPOHP:0001249
- 2 of 2 reported patients
- Delayed CNS myelinationHPOHP:0002188
- 1 of 2 reported patients
- EpicanthusHPOHP:0000286
- 1 of 2 reported patients
- EsotropiaHPOHP:0000565
- 1 of 2 reported patients
- Focal-onset seizureHPOHP:0007359
- 1 of 2 reported patients
- High palateHPOHP:0000218
- 1 of 2 reported patients
- HypertelorismHPOHP:0000316
- 1 of 2 reported patients
- Myoclonic seizureHPOHP:0032794
- 1 of 2 reported patients
- Short statureHPOHP:0004322
- 1 of 2 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.
- NCDNHGNC:17597
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2021
- Strong · PanelApp Australia · Autosomal dominant · 2025
- Strong · PanelApp Australia · Autosomal recessive · 2025
- Strong · G2P · Autosomal dominant · 2021