Multiple congenital anomalies-neurodevelopmental syndrome, x-linked

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Subtype of: Multiple congenital anomalies
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Multiple congenital anomalies-neurodevelopmental syndrome, X-linked
MONDO_0025351
OTUD5 Causal
33131077 33523931
ClinGen, Open Targets
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Multiple congenital anomalies-neurodevelopmental syndrome, x-linked.
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Dysgenesis of corpus callosum 1 shared geneOTUD5 Related via 1 shared gene including OTUD5. Non-specific syndromic intellectual disability 1 shared geneOTUD5 Related via 1 shared gene including OTUD5. Neurodevelopmental disorder 1 shared geneOTUD5 Related via 1 shared gene including OTUD5.