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Rotor syndrome
Rotor syndrome
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Pathways column key:
KEGG
Reactome
Disease Term
Disease ID
Gene Symbol
Classification
References
Source
Pathways
ROTOR SYNDROME
3111
C0220991
MONDO:0009379
SLCO1B1
Causal
22232210
23236639
ClinVar
,
Disgenet
,
GWAS catalog
,
Orphanet
Bile secretion
Folate transport and metabolism
Recycling of bile acids and salts
Heme degradation
Defective SLCO1B1 causes hyperbilirubinemia, Rotor type (HBLRR)
Transport of organic anions
+3 more
SLCO1B3
Causal
22232210
23236639
ClinVar
,
Disgenet
,
GWAS catalog
,
Orphanet
Bile secretion
Folate transport and metabolism
Recycling of bile acids and salts
Heme degradation
Defective SLCO1B3 causes hyperbilirubinemia, Rotor type (HBLRR)
Transport of organic anions
+3 more
All
3
Causal
2
Unknown
1
Select all
Clear
ClinVar
2
Orphanet
2
Disgenet
2
CTD
0
HPO
0
GWAS catalog
2
GenCC
0
ClinGen
0
Related Diseases
Diseases that share the most curated genes with Rotor syndrome.
5
View disease cluster →
Hyperbilirubinemia
2 shared genes
SLCO1B1, SLCO1B3
Related via 2 shared genes including SLCO1B1, SLCO1B3.
Gilbert syndrome
1 shared gene
SLCO1B1
Related via 1 shared gene including SLCO1B1.
Bilirubin metabolism disease
1 shared gene
SLCO1B1
Related via 1 shared gene including SLCO1B1.
Chagas cardiomyopathy
1 shared gene
SLCO1B1
Related via 1 shared gene including SLCO1B1.
Hypogonadism
1 shared gene
SLCO1B1
Related via 1 shared gene including SLCO1B1.
1
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