Multiple congenital anomalies

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
KAT6B-related multiple congenital anomalies syndrome
KAT6B Causal — ClinGen
All7 Causal1 Unknown6
Related Diseases Diseases that share the most curated genes with Multiple congenital anomalies.
5 View disease cluster →
Complex neurodevelopmental disorder with or without congenital anomalies 2 shared genesMYH10, TRRAP Related via 2 shared genes including MYH10, TRRAP. Simpson syndrome 1 shared geneKAT6B Related via 1 shared gene including KAT6B. Genitopatellar syndrome 1 shared geneKAT6B Related via 1 shared gene including KAT6B. Sbbyss syndrome 1 shared geneKAT6B Related via 1 shared gene including KAT6B. KAT6B-related disorders 1 shared geneKAT6B Related via 1 shared gene including KAT6B.