neurodevelopmental disorder with visual defects and brain anomalies
MONDO:0032807Mondo
Findings
No curated finding names neurodevelopmental disorder with visual defects and brain anomalies yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal dominant inheritance
HPO, annotations 2026-09-02
Features
38 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.
- Global developmental delayHPOHP:0001263
- 7 of 7 reported patients
- Intellectual disabilityHPOHP:0001249
- 5 of 5 reported patients
- Hypoplasia of the corpus callosumHPOHP:0002079
- 6 of 7 reported patients
- Delayed speech and language developmentHPOHP:0000750
- 4 of 5 reported patients
- AtaxiaHPOHP:0001251
- 3 of 4 reported patients
- Delayed ability to sitHPOHP:0025336
- 4 of 6 reported patients
- Optic atrophyHPOHP:0000648
- 4 of 7 reported patients
- Feeding difficultiesHPOHP:0011968
- 3 of 7 reported patients
- Rod-cone dystrophyHPOHP:0000510
- 3 of 7 reported patients
- Delayed ability to walkHPOHP:0031936
- 2 of 7 reported patients
- Infantile spasmsHPOHP:0012469
- 2 of 7 reported patients · Infantile onset
- LaryngotracheomalaciaHPOHP:0008755
- 2 of 7 reported patients · Congenital onset
Show the remaining 26
- Limb hypertoniaHPOHP:0002509
- 2 of 7 reported patients
- Pes planusHPOHP:0001763
- 2 of 7 reported patients
- Respiratory tract infectionHPOHP:0011947
- 2 of 7 reported patients
- ScoliosisHPOHP:0002650
- 2 of 7 reported patients
- Short statureHPOHP:0004322
- 2 of 7 reported patients
- StrabismusHPOHP:0000486
- 2 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.
- HK1HGNC:4922
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2023
- Strong · G2P · Autosomal dominant · 2025
- Strong · PanelApp Australia · Autosomal dominant · 2025
- Moderate · Ambry Genetics · Autosomal dominant · 2020