developmental delay, language impairment, and ocular abnormalities
MONDO:0859324Mondo
Findings
No curated finding names developmental delay, language impairment, and ocular 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
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.
- Delayed speech and language developmentHPOHP:0000750
- 7 of 7 reported patients
- MicrocephalyHPOHP:0000252
- 6 of 7 reported patients
- Motor delayHPOHP:0001270
- 6 of 7 reported patients
- StrabismusHPOHP:0000486
- 4 of 7 reported patients
- Attention deficit hyperactivity disorderHPOHP:0007018
- 2 of 7 reported patients
- Cerebral visual impairmentHPOHP:0100704
- 2 of 7 reported patients
- Facial telangiectasiaHPOHP:0007380
- 2 of 7 reported patients
- Accommodative esotropiaHPOHP:0020046
- 1 of 7 reported patients
- Aggressive behaviorHPOHP:0000718
- 1 of 7 reported patients
- ApraxiaHPOHP:0002186
- 1 of 7 reported patients
- Contracture of the proximal interphalangeal joint of the 5th fingerHPOHP:0009185
- 1 of 7 reported patients
- Developmental cataractHPOHP:0000519
- 1 of 7 reported patients
Show the remaining 14
- ExotropiaHPOHP:0000577
- 1 of 7 reported patients
- Frequent temper tantrumsHPOHP:0025161
- 1 of 7 reported patients
- HyperactivityHPOHP:0000752
- 1 of 7 reported patients
- ImpulsivityHPOHP:0100710
- 1 of 7 reported patients
- Inguinal herniaHPOHP:0000023
- 1 of 7 reported patients
- Motor stereotypyHPOHP:0000733
- 1 of 7 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.
- ARPC4HGNC:707
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2023
- Strong · G2P · Autosomal dominant · 2025
- Strong · PanelApp Australia · Autosomal dominant · 2025
- Moderate · Ambry Genetics · Autosomal dominant · 2022
Where it sits
- A kind of