TCF7L2-related neurodevelopmental disorder
MONDO:0100525Mondo
Findings
No curated finding names TCF7L2-related neurodevelopmental disorder yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
A newly discovered disorder caused by a change (variant or mutation) in the TCF7L2 gene. This mutation may be responsible for developmental delays in childhood, intellectual disability, autism, myopia, ADHD, abnormal physical features and other problems. There is a wide spectrum of severity for individuals affected with TRND. Many of the symptoms of TRND overlap with other neurodevelopmental disorders. TRND must be diagnosed with a genetic test and cannot be diagnosed by symptoms alone.
Definition from the Mondo Disease Ontology (MONDO:0100525), read 2026-09-29. CC BY 4.0.
Where it sits
- A kind of