KAT6B-related multiple congenital anomalies syndrome

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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
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with KAT6B-related multiple congenital anomalies syndrome.
5 View disease cluster →
Simpson syndrome 1 shared geneKAT6B Related via 1 shared gene including KAT6B. Hereditary angiopathy with nephropathy, aneurysms, and muscle cramps 1 shared geneKAT6B Related via 1 shared gene including KAT6B. Blepharophimosis syndrome 1 shared geneKAT6B Related via 1 shared gene including KAT6B. Blepharophimosis-intellectual disability syndrome 1 shared geneKAT6B Related via 1 shared gene including KAT6B. Neuropathic spinal arthropathy 1 shared geneKAT6B Related via 1 shared gene including KAT6B.