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DOID:13269 - hereditary coproporphyria
Disease Ontology Definition:n_a
Synonyms: Coproporphyrinogen oxidase deficiency, Hereditary coproporphyria, Hereditary coproporphyria (disorder), hereditary coproporphyria porphyria,
Echinobase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MIM:121300 - coproporphyria, hereditary; hcp |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
acute porphyria (is_a)