ARF3-related neurodevelopmental disorder
MONDO:0700366Mondo
Findings
No curated finding names ARF3-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 ARF3 gene. This disorder is characterised by intellectual disability, delayed or absent speech, motor development delay, and brain MRI abnormalitites. Other phenotypes observed less frequently include seizures, hypotonia, acquired microcephaly, dysmorphic features, and cardiac abnormalities.
Definition from the Mondo Disease Ontology (MONDO:0700366), read 2026-09-29. CC BY 4.0.