intellectual developmental disorder with ocular anomalies and distinctive facial features
MONDO:0859303Mondo
Findings
No curated finding names intellectual developmental disorder with ocular anomalies and distinctive facial features 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
HPO, annotations 2026-09-02
Features
14 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.
- EpicanthusHPOHP:0000286
- 4 of 4 reported patients
- Global developmental delayHPOHP:0001263
- 5 of 5 reported patients
- Mild intellectual disabilityHPOHP:0001256
- 3 of 3 reported patients
- Narrow foreheadHPOHP:0000341
- 4 of 4 reported patients
- Upslanted palpebral fissureHPOHP:0000582
- 4 of 4 reported patients
- Autistic behaviorHPOHP:0000729
- 2 of 3 reported patients
- NystagmusHPOHP:0000639
- 3 of 5 reported patients
- Sensorineural hearing impairmentHPOHP:0000407
- 2 of 4 reported patients
- MicrocephalyHPOHP:0000252
- 2 of 5 reported patients
- PtosisHPOHP:0000508
- 2 of 5 reported patients
- Hypoplasia of the foveaHPOHP:0007750
- 1 of 5 reported patients
- Iris cystHPOHP:0011523
- 1 of 5 reported patients
Show the remaining 2
- Optic atrophyHPOHP:0000648
- 1 of 5 reported patients
- SeizureHPOHP:0001250
- 1 of 5 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.
- HGNC:25094HGNC:25094
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2023
- Strong · PanelApp Australia · Autosomal dominant · 2025
- Moderate · Ambry Genetics · Autosomal dominant · 2024
- Moderate · G2P · Autosomal dominant · 2022
Where it sits
- A kind of