Intellectual disability-facial dysmorphism syndrome due to setd5 haploinsufficiency

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Subtype of: Facial dysmorphism syndrome · Intellectual disability
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency
MONDO_0014336
SETD5 Causal
31474762 23020937 24680889 25138099
Open Targets —
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Intellectual disability-facial dysmorphism syndrome due to setd5 haploinsufficiency.
5 View disease cluster →
Mental retardation, autosomal dominant 23 1 shared geneSETD5 Related via 1 shared gene including SETD5. Intellectual developmental disorder, autosomal dominant 23 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.