GRIN2B-related complex neurodevelopmental disorder
MONDO:0700350Mondo
Findings
No curated finding names GRIN2B-related complex neurodevelopmental disorder yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
A complex neurodevelopmental disorder caused by a variation in the GRIN2B gene
Definition from the Mondo Disease Ontology (MONDO:0700350), read 2026-09-29. CC BY 4.0.
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.
- GRIN2BHGNC:4586
- Strong · PanelApp Australia · Autosomal dominant · 2025