Mental retardation, autosomal dominant 19

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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 19
MONDO_0014035
CTNNB1 Unknown
27915094 30929091 28514307 26968164 25326669 35880249 24614104
Open Targets
Rap1 signaling pathway Wnt signaling pathway Hippo signaling pathway +51 more
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Mental retardation, autosomal dominant 19.
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Intellectual developmental disorder dysmorphic ocular microcephaly peripheral 1 shared geneCTNNB1 Related via 1 shared gene including CTNNB1. Neurodevelopmental disorder and/or vitreoretinopathy 1 shared geneCTNNB1 Related via 1 shared gene including CTNNB1. Fibrosarcoma 1 shared geneCTNNB1 Related via 1 shared gene including CTNNB1. Colorectal hamartoma 1 shared geneCTNNB1 Related via 1 shared gene including CTNNB1. Ovarian endometrioid adenocarcinoma with squamous differentiation 1 shared geneCTNNB1 Related via 1 shared gene including CTNNB1.