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intellectual developmental disorder with or without epilepsy or cerebellar ataxia

Disease Summary
Associated Targets (1)
Tchem

1


Uniprot Description An autosomal dominant neurodevelopmental disorder that manifests with variable features of mild-to-severe intellectual disability, developmental delay, autism spectrum disorder, cerebellar ataxia and epilepsy.
Mondo Term and Equivalent IDs
MONDO:0060745:  intellectual developmental disorder with or without epilepsy or cerebellar ataxia
UMLS:CN252646: