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Congenital heart disease with heterotaxy syndrome
Congenital heart disease with heterotaxy syndrome
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Subtype of:
Congenital heart disease
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Pathways column key:
KEGG
Reactome
Disease Term
Disease ID
Gene Symbol
Classification
References
Source
Pathways
congenital heart disease with heterotaxy syndrome
NODAL
Unknown
—
ClinGen
Cytokine-cytokine receptor interaction
TGF-beta signaling pathway
Signaling pathways regulating pluripotency of stem cells
ZIC3
Unknown
—
ClinGen
Signaling pathways regulating pluripotency of stem cells
POU5F1 (OCT4), SOX2, NANOG activate genes related to proliferation
Transcriptional regulation of pluripotent stem cells
All
2
Causal
0
Unknown
2
Select all
Clear
ClinVar
0
Orphanet
0
Disgenet
0
CTD
0
HPO
0
GWAS catalog
0
GenCC
0
ClinGen
2
Open Targets
0
Related Diseases
Diseases that share the most curated genes with Congenital heart disease with heterotaxy syndrome.
5
View disease cluster →
VACTERL association, X-linked
1 shared gene
ZIC3
Related via 1 shared gene including ZIC3.
Heterotaxy, visceral, 1, x-linked
1 shared gene
ZIC3
Related via 1 shared gene including ZIC3.
Congenital heart defects, multiple types, 1, x-linked
1 shared gene
ZIC3
Related via 1 shared gene including ZIC3.
Dextrocardia
1 shared gene
ZIC3
Related via 1 shared gene including ZIC3.
Situs inversus
2 shared genes
ZIC3, NODAL
Related via 2 shared genes including ZIC3, NODAL.
1
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