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autosomal dominant polycystic kidney disease
autosomal dominant polycystic kidney disease
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Pathways column key:
KEGG
Reactome
Disease Term
Disease ID
Gene Symbol
Classification
References
Source
Pathways
autosomal dominant polycystic kidney disease
DNAJB11
Causal
—
ClinGen
Protein processing in endoplasmic reticulum
XBP1(S) activates chaperone genes
IFT140
Causal
—
ClinGen
Hedgehog 'off' state
Intraflagellar transport
PKD1
Causal
—
ClinGen
VxPx cargo-targeting to cilium
PKD2
Causal
28356211
23431072
ClinGen
VxPx cargo-targeting to cilium
All
7
Causal
4
Unknown
3
Select all
Clear
ClinVar
0
Orphanet
0
Disgenet
0
CTD
0
HPO
0
GWAS catalog
0
GenCC
0
ClinGen
4
Related Diseases
Diseases that share the most curated genes with autosomal dominant polycystic kidney disease.
5
View disease cluster →
Anhydramnios
3 shared genes
DNAJB11, PKD1, PKD2
Related via 3 shared genes including DNAJB11, PKD1, PKD2.
Polycystic kidney disease
7 shared genes
ALG8, DNAJB11, PKD1, PKD2, IFT140, ALG5, NEK8
Related via 7 shared genes including ALG8, DNAJB11, PKD1.
Liver cyst
1 shared gene
PKD1
Related via 1 shared gene including PKD1.
IFT140-related recessive ciliopathy
1 shared gene
IFT140
Related via 1 shared gene including IFT140.
renal-hepatic-pancreatic dysplasia 2
1 shared gene
NEK8
Related via 1 shared gene including NEK8.
1
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