Mental retardation, autosomal dominant 51

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Subtype of: Intellectual disability
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Pathways column key: KEGG Reactome
Disease terms Disease ID Gene Symbol Classification References Source Pathways
  • Mental retardation, autosomal dominant 51
MONDO_0030917
KMT5B Unknown
25363768 28191889 29276005
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Mental retardation, autosomal dominant 51.
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Intellectual developmental disorder dysmorphic hypotonia 1 shared geneKMT5B Related via 1 shared gene including KMT5B. Intellectual developmental disorder, autosomal dominant 51 1 shared geneKMT5B Related via 1 shared gene including KMT5B. Neural tube defect 1 shared geneKMT5B Related via 1 shared gene including KMT5B. Complex neurodevelopmental disorder 1 shared geneKMT5B Related via 1 shared gene including KMT5B. Non-specific syndromic intellectual disability 1 shared geneKMT5B Related via 1 shared gene including KMT5B.