neurodevelopmental disorder with or without variable movement or behavioral abnormalities
MONDO:0859225Mondo
Findings
No curated finding names neurodevelopmental disorder with or without variable movement or behavioral abnormalities 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 · Childhood onset
HPO, annotations 2026-09-02
Features
27 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.
- Intellectual disabilityHPOHP:0001249
- 9 of 9 reported patients
- Global developmental delayHPOHP:0001263
- 9 of 10 reported patients
- Motor delayHPOHP:0001270
- 9 of 10 reported patients
- Delayed speech and language developmentHPOHP:0000750
- 8 of 10 reported patients
- Autistic behaviorHPOHP:0000729
- 6 of 10 reported patients
- AtaxiaHPOHP:0001251
- 4 of 10 reported patients
- Intention tremorHPOHP:0002080
- 4 of 10 reported patients
- AnxietyHPOHP:0000739
- 3 of 10 reported patients
- Attention deficit hyperactivity disorderHPOHP:0007018
- 3 of 10 reported patients
- Motor ticsHPOHP:0100034
- 3 of 10 reported patients
- Bilateral tonic-clonic seizureHPOHP:0002069
- 2 of 10 reported patients
- DyskinesiaHPOHP:0100660
- 2 of 10 reported patients
Show the remaining 15
- Resting tremorHPOHP:0002322
- 2 of 10 reported patients
- Abnormal periventricular white matter morphologyHPOHP:0002518
- 1 of 10 reported patients
- BradykinesiaHPOHP:0002067
- 1 of 10 reported patients
- ChoreaHPOHP:0002072
- 1 of 10 reported patients
- Cogwheel rigidityHPOHP:0002396
- 1 of 10 reported patients · Juvenile onset
- Delayed CNS myelinationHPOHP:0002188
- 1 of 10 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.
- KCNN2HGNC:6291
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2022
- Strong · PanelApp Australia · Autosomal dominant · 2025
- Moderate · G2P · Autosomal dominant · 2025