Skip to content
GenoLensGenoLens

complex neurodevelopmental disorder

MONDO:0100038

Also known as: complex neurodevelopmental disorder

MONDO:
MONDO:0100038
Orphanet:
528084
Rare disease207 associated genes

Description

A disorder that involves more than one phenotype associated with the central nervous system, including but not limited to intellectual disability, autism, and seizures (epilepsy).

Associated genes

+197 more genes — install the extension to see the full list inline on any page.

External references

Sources: MONDO (CC BY 4.0), Open Targets (CC0), Orphanet (CC BY 4.0).

Not for sole clinical decision-making. Always verify against primary sources.