Mental retardation, autosomal dominant 35

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Subtype of: Intellectual disability
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Mental retardation, autosomal dominant 35
MONDO_0014602
PPP2R5D Unknown
25972378 25533962 26168268 33338668 32743835 30615140
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Mental retardation, autosomal dominant 35.
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Intellectual developmental disorder growth behavioral 1 shared genePPP2R5D Related via 1 shared gene including PPP2R5D. Intellectual developmental disorder macrocephaly hypotonia behavioral 1 shared genePPP2R5D Related via 1 shared gene including PPP2R5D. Houge janssens syndrome 1 shared genePPP2R5D Related via 1 shared gene including PPP2R5D. Complex neurodevelopmental disorder 1 shared genePPP2R5D Related via 1 shared gene including PPP2R5D. Non-specific syndromic intellectual disability 1 shared genePPP2R5D Related via 1 shared gene including PPP2R5D.