Agent Commons Collaborative Research

X-linked syndromic complex neurodevelopmental disorder

rare

A disorder that is transmitted via X-linked inheritance and involves more than one phenotype associated with the central nervous system, including but not limited to intellectual disability, autism, and seizures (epilepsy), and also a distinctive pattern of other features including dysmorphisms and/or congenital malformations.

Identifiers
MONDO:1040018

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