neurodevelopmental disorder with dysmorphic facies and cerebellar hypoplasia
MONDO:0859141Mondo
Findings
No curated finding names neurodevelopmental disorder with dysmorphic facies and cerebellar hypoplasia 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 · Infantile onset
HPO, annotations 2026-09-02
Features
34 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.
- Depressed nasal tipHPOHP:0000437
- 2 of 3 reported patients
- Flexion contractureHPOHP:0001371
- 2 of 3 reported patients
- HypertelorismHPOHP:0000316
- 2 of 3 reported patients
- Secondary microcephalyHPOHP:0005484
- 2 of 3 reported patients
- Severe global developmental delayHPOHP:0011344
- 2 of 3 reported patients
- Sloping foreheadHPOHP:0000340
- 2 of 3 reported patients
- Spastic tetraplegiaHPOHP:0002510
- 2 of 3 reported patients
- Thin upper lip vermilionHPOHP:0000219
- 2 of 3 reported patients
- Upslanted palpebral fissureHPOHP:0000582
- 2 of 3 reported patients
- Cerebellar vermis hypoplasiaHPOHP:0001320
- 3 of 6 reported patients
- Accessory spleenHPOHP:0001747
- 1 of 3 reported patients
- Bitemporal hollowingHPOHP:0025386
- 1 of 3 reported patients
Show the remaining 22
- Central nervous system cystHPOHP:0030724
- 1 of 3 reported patients
- Cerebellar hypoplasiaHPOHP:0001321
- 1 of 3 reported patients
- CNS hypomyelinationHPOHP:0003429
- 1 of 3 reported patients
- Dilated fourth ventricleHPOHP:0002198
- 1 of 3 reported patients
- Dry skinHPOHP:0000958
- 1 of 3 reported patients
- Exaggerated cupid's bowHPOHP:0002263
- 1 of 3 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.
- EXOC2HGNC:24968
- Moderate · PanelApp Australia · Autosomal recessive · 2025
- Limited · Labcorp Genetics (formerly Invitae) · Unknown · 2021