Adams-oliver syndrome

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
ADAMS-OLIVER SYNDROME
MONDO:0007034
DLL4 Causal
26299364
CTD
DOCK6 Causal
17196961 21820096 23522784 25091416 25824905 28884918 29631299 29924900 30898718 31654484 33655927
GWAS catalog
EOGT Causal
23522784
Disgenet
NOTCH1 Causal
10837027 16025100 18593716 25132448 26820064 29924900
GWAS catalog
ADAMS-OLIVER SYNDROME 1
MONDO:0024506
ARHGAP31 Causal
16451141 474617
Disgenet
ADAMS-OLIVER SYNDROME 2
MONDO:0013635
DOCK6 Causal
21820096 28884918 30898718 32498638
Disgenet, ClinGen
ADAMS-OLIVER SYNDROME 3
MONDO:0013895
RBPJ Causal
22883147 240680 29924900
GWAS catalog
ADAMS-OLIVER SYNDROME 4
MONDO:0014124
EOGT Causal
23522784
ClinVar, ClinGen
ADAMS-OLIVER SYNDROME 5
MONDO:0014459
NOTCH1 Causal — GenCC
ADAMS-OLIVER SYNDROME 6
MONDO:0014703
DLL4 Causal
26299364
Disgenet
All6 Causal6 Unknown2
Related Diseases Diseases that share the most curated genes with Adams-oliver syndrome.
5 View disease cluster →
NOTCH1-related AOS spectrum disorder 1 shared geneNOTCH1 Related via 1 shared gene including NOTCH1. Aplasia cutis congenita 1 shared geneDLL4 Related via 1 shared gene including DLL4. Congenital abnormalities 1 shared geneNOTCH1 Related via 1 shared gene including NOTCH1. Congenital hydrocephalus 1 shared geneDOCK6 Related via 1 shared gene including DOCK6. Bicuspid aortic valve 1 shared geneNOTCH1 Related via 1 shared gene including NOTCH1.