neurodevelopmental disorder with epilepsy and brain atrophy
MONDO:0859265Mondo
Findings
No curated finding names neurodevelopmental disorder with epilepsy and brain atrophy yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal recessive inheritance
- Onset and course
- Infantile onset · Juvenile onset · Neonatal onset · Young adult onset
HPO, annotations 2026-09-02
Features
22 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.
- AtaxiaHPOHP:0001251
- 5 of 5 reported patients
- Global developmental delayHPOHP:0001263
- 2 of 2 reported patients
- Intellectual disabilityHPOHP:0001249
- 5 of 5 reported patients
- Mandibular prognathiaHPOHP:0000303
- 4 of 4 reported patients
- MyoclonusHPOHP:0001336
- 5 of 5 reported patients
- SeizureHPOHP:0001250
- 7 of 7 reported patients
- Atrophy/Degeneration affecting the brainstemHPOHP:0007366
- 1 of 2 reported patients
- Attention deficit hyperactivity disorderHPOHP:0007018
- 1 of 2 reported patients
- Cerebellar atrophyHPOHP:0001272
- 1 of 2 reported patients
- Cerebellar hypoplasiaHPOHP:0001321
- 1 of 2 reported patients
- Cortical dysplasiaHPOHP:0002539
- 1 of 2 reported patients
- EEG with burst suppressionHPOHP:0010851
- 1 of 2 reported patients
Show the remaining 10
- Epileptic spasmHPOHP:0011097
- 1 of 2 reported patients
- Erratic myoclonusHPOHP:0025357
- 1 of 2 reported patients
- Feeding difficultiesHPOHP:0011968
- 1 of 2 reported patients
- Gastroesophageal refluxHPOHP:0002020
- 1 of 2 reported patients
- Intermittent diarrheaHPOHP:0002254
- 1 of 2 reported patients
- MalnutritionHPOHP:0004395
- 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.
- ATP6V0A1HGNC:865
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2022
- Moderate · Ambry Genetics · Autosomal recessive · 2022