neurodevelopmental disorder with midbrain and hindbrain malformations
MONDO:0056797Mondo
Findings
No curated finding names neurodevelopmental disorder with midbrain and hindbrain malformations 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
- Congenital onset
HPO, annotations 2026-09-02
Features
26 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.
- AstigmatismHPOHP:0000483
- 2 of 2 reported patients
- Delayed speech and language developmentHPOHP:0000750
- 2 of 2 reported patients
- Frequent fallsHPOHP:0002359
- 2 of 2 reported patients
- Hypoplasia of the ponsHPOHP:0012110
- 2 of 2 reported patients
- HyporeflexiaHPOHP:0001265
- 2 of 2 reported patients
- HypotoniaHPOHP:0001252
- 2 of 2 reported patients
- Intellectual disabilityHPOHP:0001249
- 2 of 2 reported patients
- Long eyelashesHPOHP:0000527
- 2 of 2 reported patients
- Primary microcephalyHPOHP:0011451
- 2 of 2 reported patients · Congenital onset
- StrabismusHPOHP:0000486
- 2 of 2 reported patients · Congenital onset
- Abnormal auditory evoked potentialsHPOHP:0006958
- 1 of 2 reported patients
- Abnormality of visual evoked potentialsHPOHP:0000649
- 1 of 2 reported patients
Show the remaining 14
- AmblyopiaHPOHP:0000646
- 1 of 2 reported patients
- Broad fingerHPOHP:0001500
- 1 of 2 reported patients
- Cerebellar vermis hypoplasiaHPOHP:0001320
- 1 of 2 reported patients
- Downslanted palpebral fissuresHPOHP:0000494
- 1 of 2 reported patients
- High palateHPOHP:0000218
- 1 of 2 reported patients
- Horizontal pendular nystagmusHPOHP:0007811
- 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.
- ARHGEF2HGNC:682
- Limited · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2020
Where it sits
Other names
1 name
Resolves to: neurodevelopmental disorder with midbrain and hindbrain malformations
- Also called
- NEDMHM