Intellectual developmental disorder, autosomal dominant 5

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Subtype of: Intellectual developmental disorder
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Pathways column key: KEGG Reactome
Disease terms Disease ID Gene Symbol Classification References Source Pathways
  • Intellectual developmental disorder, autosomal dominant 5
MONDO_0012960
SYNGAP1 Unknown
19196676 21076407 21237447 23161826 23708187
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Intellectual developmental disorder, autosomal dominant 5.
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Mental retardation autosomal dominant type 5 1 shared geneSYNGAP1 Related via 1 shared gene including SYNGAP1. Epilepsy with myoclonic atonic seizures 1 shared geneSYNGAP1 Related via 1 shared gene including SYNGAP1. Blepharoptosis 1 shared geneSYNGAP1 Related via 1 shared gene including SYNGAP1. Cerebellar ataxia 1 shared geneSYNGAP1 Related via 1 shared gene including SYNGAP1. Complex neurodevelopmental disorder 1 shared geneSYNGAP1 Related via 1 shared gene including SYNGAP1.