rolandic epilepsy, intellectual disability, and speech dyspraxia, X-linked
MONDO:0010388Mondo
Findings
No curated finding names rolandic epilepsy, intellectual disability, and speech dyspraxia, X-linked 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
1 feature
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.
- Bilateral perisylvian polymicrogyriaHPOHP:0032407
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.
- SRPX2HGNC:30668
- Limited · Labcorp Genetics (formerly Invitae) · X-linked · 2021
- Limited · PanelApp Australia · X-linked · 2025
- Disputed Evidence · Ambry Genetics · X-linked · 2019
Where it sits
Other names
2 names
Resolves to: rolandic epilepsy, intellectual disability, and speech dyspraxia, X-linked
- Also called
- rolandic epilepsy, impaired intellectual development, and speech dyspraxiarolandic epilepsy, mental retardation, and speech dyspraxia, X-linked