neurodevelopmental disorder with dystonia and seizures
MONDO:0859258Mondo
Findings
No curated finding names neurodevelopmental disorder with dystonia and seizures 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 · Fetal onset · Third trimester onset
HPO, annotations 2026-09-02
Features
23 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.
- Absent speechHPOHP:0001344
- 2 of 2 reported patients
- AnxietyHPOHP:0000739
- 2 of 2 reported patients
- AthetosisHPOHP:0002305
- 2 of 2 reported patients
- Cerebellar hypoplasiaHPOHP:0001321
- 1 of 1 reported patient
- Cerebral cortical atrophyHPOHP:0002120
- 1 of 1 reported patient
- ChoreaHPOHP:0002072
- 2 of 2 reported patients
- ConstipationHPOHP:0002019
- 2 of 2 reported patients
- Decreased fetal movementHPOHP:0001558
- 1 of 1 reported patient
- DystoniaHPOHP:0001332
- 2 of 2 reported patients
- Feeding difficultiesHPOHP:0011968
- 1 of 1 reported patient
- Global developmental delayHPOHP:0001263
- 3 of 3 reported patients
- HyperhidrosisHPOHP:0000975
- 2 of 2 reported patients
Show the remaining 11
- HypotoniaHPOHP:0001252
- 2 of 2 reported patients
- Intrauterine growth retardationHPOHP:0001511
- 1 of 1 reported patient
- SeizureHPOHP:0001250
- 3 of 3 reported patients
- Self-injurious behaviorHPOHP:0100716
- 2 of 2 reported patients
- Spastic tetraplegiaHPOHP:0002510
- 1 of 1 reported patient
- Temperature instabilityHPOHP:0005968
- 2 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.
- SHQ1HGNC:25543
- Strong · Ambry Genetics · Autosomal recessive · 2024
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2023
- Strong · PanelApp Australia · Autosomal recessive · 2025