Mental retardation, autosomal dominant 23

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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 23
MONDO_0014336
SETD5 Unknown
29484850 24680889 25138099 31474762 23020937 28549204 27375234 28905509 31656537 28881385
Open Targets —
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Mental retardation, autosomal dominant 23.
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Intellectual developmental disorder, autosomal dominant 23 1 shared geneSETD5 Related via 1 shared gene including SETD5. Intellectual disability-facial dysmorphism syndrome due to setd5 haploinsufficiency 1 shared geneSETD5 Related via 1 shared gene including SETD5. Intellectual developmental disorder dysmorphic facial 1 shared geneSETD5 Related via 1 shared gene including SETD5. Hyperphosphatasia with intellectual disability syndrome 1 shared geneSETD5 Related via 1 shared gene including SETD5. Facial dysmorphism syndrome 1 shared geneSETD5 Related via 1 shared gene including SETD5.