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autosomal dominant medullary cystic kidney disease with or without hyperuricemia
autosomal dominant medullary cystic kidney disease with or without hyperuricemia
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Pathways column key:
KEGG
Reactome
Disease Term
Disease ID
Gene Symbol
Classification
References
Source
Pathways
autosomal dominant medullary cystic kidney disease with or without hyperuricemia
UMOD
Causal
—
ClinGen
Asparagine N-linked glycosylation
APOA4
Unknown
—
ClinGen
Fat digestion and absorption
Vitamin digestion and absorption
Cholesterol metabolism
Lipid and atherosclerosis
+1 more
All
2
Causal
1
Unknown
1
Select all
Clear
ClinVar
0
Orphanet
0
Disgenet
0
CTD
0
HPO
0
GWAS catalog
0
GenCC
0
ClinGen
2
Related Diseases
Diseases that share the most curated genes with autosomal dominant medullary cystic kidney disease with or without hyperuricemia.
5
View disease cluster →
Juvenile hyperuricemic nephropathy
1 shared gene
UMOD
Related via 1 shared gene including UMOD.
Tubulointerstitial kidney disease
2 shared genes
APOA4, UMOD
Related via 2 shared genes including APOA4, UMOD.
Hyperuricemic nephropathy
1 shared gene
UMOD
Related via 1 shared gene including UMOD.
Hypertensive heart disease
1 shared gene
UMOD
Related via 1 shared gene including UMOD.
Hydronephrosis
1 shared gene
UMOD
Related via 1 shared gene including UMOD.
1
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