hereditary coproporphyria Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_13269)
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11 genes co-occuring with the disease hereditary coproporphyria in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
CPOX coproporphyrinogen oxidase 3.51916
UROS uroporphyrinogen III synthase 2.3737
FECH ferrochelatase 1.76547
HMBS hydroxymethylbilane synthase 1.75686
ALAD aminolevulinate dehydratase 1.74142
UROD uroporphyrinogen decarboxylase 1.73778
PPOX protoporphyrinogen oxidase 1.72958
ALAS1 5'-aminolevulinate synthase 1 0.596402
ALAS2 5'-aminolevulinate synthase 2 0.563723
STS steroid sulfatase (microsomal), isozyme S 0.381481
RNASEH2A ribonuclease H2, subunit A 0.173832