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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.
Parent term
MONDO 0800439: syndromic complex neurodevelopmental disorder
Label
X-linked syndromic complex neurodevelopmental disorder
Synonyms
No response
Synonym type
None
Definition
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.
Parent term
MONDO 0800439: syndromic complex neurodevelopmental disorder
Children term(s)
No response
ORCID Identifier
No response
Website URL
https://clinicalgenome.org/affiliation/40006/
Additional comments
@ErinRiggs
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