WDR5-related neurodevelopmental disorder
MONDO:0700365Mondo
Findings
No curated finding names WDR5-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 WDR5 gene. This disorder is characterised by speech and language delay, motor development delay and/or intellectual disability. Other phenotypic features commonly reported include hypotonia, epilepsy, and behavioural abnormalities.
Definition from the Mondo Disease Ontology (MONDO:0700365), read 2026-09-29. CC BY 4.0.