neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities
MONDO:0957386Mondo
Findings
No curated finding names neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities 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 · Neonatal onset · Childhood onset
HPO, annotations 2026-09-02
Features
42 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.
- Agenesis of corpus callosumHPOHP:0001274
- 1 of 1 reported patient
- AstigmatismHPOHP:0000483
- 1 of 1 reported patient
- Bifid uvulaHPOHP:0000193
- 1 of 1 reported patient
- Brain atrophyHPOHP:0012444
- 1 of 1 reported patient
- Cerebellar atrophyHPOHP:0001272
- 4 of 4 reported patients
- Cerebellar hypoplasiaHPOHP:0001321
- 3 of 3 reported patients
- Cerebral atrophyHPOHP:0002059
- 3 of 3 reported patients
- Coarse facial featuresHPOHP:0000280
- 4 of 4 reported patients
- CraniosynostosisHPOHP:0001363
- 1 of 1 reported patient
- Delayed CNS myelinationHPOHP:0002188
- 1 of 1 reported patient
- Delayed speech and language developmentHPOHP:0000750
- 15 of 15 reported patients
- Dilated fourth ventricleHPOHP:0002198
- 1 of 1 reported patient
Show the remaining 30
- EpicanthusHPOHP:0000286
- 1 of 1 reported patient
- Hyperintensity of cerebral white matter on MRIHPOHP:0030890
- 1 of 1 reported patient
- HypertelorismHPOHP:0000316
- 2 of 2 reported patients
- HypotoniaHPOHP:0001252
- 10 of 10 reported patients
- Intrauterine growth retardationHPOHP:0001511
- 5 of 5 reported patients
- LeukoencephalopathyHPOHP:0002352
- 1 of 1 reported patient
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.
- INTS11HGNC:26052
- Strong · PanelApp Australia · Autosomal recessive · 2025
- Moderate · G2P · Autosomal recessive · 2025