CBX1-related neurodevelopmental disorder
MONDO:0700367Mondo
Findings
No curated finding names CBX1-related neurodevelopmental disorder yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
A neurodevelopmental disorder caused by variation in the CBX1 gene. This disorder is characterised by global motor and language developmental delay, intellectual disability, hypotonia, autism spectrum disorder, and variable dysmorphic features.
Definition from the Mondo Disease Ontology (MONDO:0700367), read 2026-09-29. CC BY 4.0.