neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy
MONDO:0060621Mondo
Findings
No curated finding names neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy 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 · Infantile onset · Progressive
HPO, annotations 2026-09-02
Features
37 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.
- Absent speechHPOHP:0001344
- 2 of 2 reported patients
- Cerebral atrophyHPOHP:0002059
- 2 of 2 reported patients
- Cerebral cortical atrophyHPOHP:0002120
- 3 of 3 reported patients
- Hypoplasia of the corpus callosumHPOHP:0002079
- 2 of 2 reported patients
- HypotoniaHPOHP:0001252
- 2 of 2 reported patients
- Intellectual disabilityHPOHP:0001249
- 2 of 2 reported patients
- MicrocephalyHPOHP:0000252
- 7 of 7 reported patients
- Motor delayHPOHP:0001270
- 2 of 2 reported patients
- Premature birthHPOHP:0001622
- 2 of 2 reported patients
- Progressive microcephalyHPOHP:0000253
- 2 of 2 reported patients
- Global developmental delayHPOHP:0001263
- 4 of 5 reported patients
- SeizureHPOHP:0001250
- 4 of 7 reported patients
Show the remaining 25
- Ankle flexion contractureHPOHP:0006466
- 1 of 2 reported patients
- Bilateral conductive hearing impairmentHPOHP:0008513
- 1 of 2 reported patients
- Breech presentationHPOHP:0001623
- 1 of 2 reported patients
- Cerebellar atrophyHPOHP:0001272
- 1 of 2 reported patients
- Depressed nasal bridgeHPOHP:0005280
- 1 of 2 reported patients
- DysphagiaHPOHP:0002015
- 1 of 2 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.
- VARS1HGNC:12651
- Definitive · ClinGen · Autosomal recessive · 2023
- Definitive · Illumina · Autosomal recessive · 2021
- Strong · PanelApp Australia · Autosomal recessive · 2025