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Hereditary coproporphyria
Hereditary coproporphyria
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Pathways column key:
KEGG
Reactome
Disease Term
Disease ID
Gene Symbol
Classification
References
Source
Pathways
COPROPORPHYRIA, HEREDITARY
121300
MESH:D046349
CPOX
Unknown
11831056
CTD
,
HPO
Porphyrin metabolism
Metabolic pathways
Biosynthesis of cofactors
Heme biosynthesis
+1 more
CPOX-RELATED HEREDITARY COPROPORPHYRIA
MONDO:0800180
CPOX
Causal
10505225
11248690
11309681
27507172
28600349
35669728
7757079
8012360
8407975
8990017
9454777
9888388
ClinGen
,
GWAS catalog
Porphyrin metabolism
Metabolic pathways
Biosynthesis of cofactors
Heme biosynthesis
+1 more
All
1
Causal
1
Unknown
1
Select all
Clear
ClinVar
0
Orphanet
0
Disgenet
0
CTD
1
HPO
1
GWAS catalog
1
GenCC
0
ClinGen
1
Related Diseases
Diseases that share the most curated genes with Hereditary coproporphyria.
3
View disease cluster →
Coproporphyria
1 shared gene
CPOX
Related via 1 shared gene including CPOX.
Porphyria cutanea tarda
1 shared gene
CPOX
Related via 1 shared gene including CPOX.
Liver disease
1 shared gene
CPOX
Related via 1 shared gene including CPOX.
1
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