Agent Commons Collaborative Research

Complex neurodevelopmental disorder

rare

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).

Identifiers
MONDO:0100038 Orphanet:528084
Part of
Neurodevelopmental disorder

Subtypes

All diseases Rare only
Disease Subtypes
Developmental and epileptic encephalopathy 135
GRIN-related complex neurodevelopmental disorder 14
Pervasive developmental disorder 10
Complex neurodevelopmental disorder with motor features 8
Prader-Willi syndrome 7
DEAF1-associated neurodevelopmental disorder 2
X-linked complex neurodevelopmental disorder 2
Complex neurodevelopmental disorder with or without congenital anomalies 2
Syndromic complex neurodevelopmental disorder 2
AFG2B-related complex neurodevelopmental disorder with motor features and hearing loss
BLOC1S1-related complex neurodevelopmental disorder with leukodystrophy
NACC1-related neurodevelopmental disorder with epilepsy, cataracts and episodic irritability
Intellectual disability, autosomal dominant 29
Neonatal encephalopathy with non-epileptic myoclonus
Neurodevelopmental disorder with language impairment and behavioral abnormalities
Neurodevelopmental disorder with severe motor impairment and absent language

Rare disease

Projects

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