neurodevelopmental disorder with microcephaly, ataxia, and seizures
MONDO:0060577Mondo
Findings
No curated finding names neurodevelopmental disorder with microcephaly, ataxia, and seizures 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
- Infantile onset
HPO, annotations 2026-09-02
Features
9 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.
- Aggressive behaviorHPOHP:0000718
- 4 of 4 reported patients
- AtaxiaHPOHP:0001251
- 4 of 4 reported patients
- Bilateral tonic-clonic seizureHPOHP:0002069
- 4 of 4 reported patients · Infantile onset
- Global developmental delayHPOHP:0001263
- 4 of 4 reported patients
- MicrocephalyHPOHP:0000252
- 4 of 4 reported patients
- Moderate intellectual disabilityHPOHP:0002342
- 4 of 4 reported patients
- Muscle weaknessHPOHP:0001324
- 4 of 4 reported patients · Juvenile onset
- Pes planusHPOHP:0001763
- 2 of 4 reported patients
- Slender buildHPOHP:0001533
- 2 of 4 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.
- SARS1HGNC:10537
- Moderate · G2P · Autosomal recessive · 2022
- Limited · ClinGen · Autosomal recessive · 2023