neurodevelopmental disorder with microcephaly, cerebral atrophy, and visual impairment
MONDO:0859293Mondo
Findings
No curated finding names neurodevelopmental disorder with microcephaly, cerebral atrophy, and visual impairment 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 · Neonatal onset
HPO, annotations 2026-09-02
Features
36 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
- 5 of 5 reported patients
- HypotoniaHPOHP:0001252
- 5 of 5 reported patients
- MicrocephalyHPOHP:0000252
- 5 of 5 reported patients
- Absent speechHPOHP:0001344
- 4 of 5 reported patients
- Thin corpus callosumHPOHP:0033725
- 4 of 5 reported patients
- Global brain atrophyHPOHP:0002283
- 3 of 5 reported patients
- NystagmusHPOHP:0000639
- 3 of 5 reported patients
- Recurrent infectionsHPOHP:0002719
- 3 of 5 reported patients
- StrabismusHPOHP:0000486
- 3 of 5 reported patients
- Delayed CNS myelinationHPOHP:0002188
- 2 of 5 reported patients
- Feeding difficultiesHPOHP:0011968
- 2 of 5 reported patients
- Generalized-onset seizureHPOHP:0002197
- 2 of 5 reported patients
Show the remaining 24
- Inability to walkHPOHP:0002540
- 2 of 5 reported patients
- Secundum atrial septal defectHPOHP:0001684
- 2 of 5 reported patients
- Ventricular septal defectHPOHP:0001629
- 2 of 5 reported patients
- Aortic regurgitationHPOHP:0001659
- 1 of 5 reported patients
- Atonic seizureHPOHP:0010819
- 1 of 5 reported patients
- Atrial septal defectHPOHP:0001631
- 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.
- DOHHHGNC:28662
- Strong · PanelApp Australia · Autosomal recessive · 2025
- Moderate · G2P · Autosomal recessive · 2022
- Limited · Ambry Genetics · Autosomal recessive · 2022