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Standards Ontologies Notations
Guidelines
MIRAGE
hereditary coproporphyria

Summary
Synonym
  • Coproporphyrinogen oxidase deficiency
  • hereditary coproporphyria porphyria
Super Class
acute porphyria digenic disease
Disease Ontology
DOID:13269
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
GARD
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
1371 CPOX coproporphyrinogen oxidase
Displaying 1 entry
Gene ID Gene Symbol Description Source
12892 Cpox coproporphyrinogen oxidase
Related Glycoprotein
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: December 8, 2025