Intellectual developmental disorder, autosomal dominant 52

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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 52
MONDO_0030918
ASH1L Unknown
23033978 25961944 27824329 28191889 28394464 32469098 34373061 34782621
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Intellectual developmental disorder, autosomal dominant 52.
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Mental retardation, autosomal dominant 52 1 shared geneASH1L Related via 1 shared gene including ASH1L. Syndromic complex neurodevelopmental disorder 1 shared geneASH1L Related via 1 shared gene including ASH1L. Lewy body disease 1 shared geneASH1L Related via 1 shared gene including ASH1L. Nonsyndromic intellectual disability 1 shared geneASH1L Related via 1 shared gene including ASH1L. Liver neoplasms 1 shared geneASH1L Related via 1 shared gene including ASH1L.