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
Multiple congenital anomalies
MONDO_0015159
CDX2 Unknown
34671974 32058622 29177441
Open Targets
FAT1 Unknown
34013115 32902815 34202629 33418956 26905694 30862798
Open Targets —
HS2ST1 Unknown
33159882
Open Targets
MYH10 Unknown
25003005 25356899 35980381
Open Targets
SLC12A2 Unknown
30740830 32754646 28940097 32658972
Open Targets
TRRAP Unknown
30827496
Open Targets
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.