Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
DOID:13269 - hereditary coproporphyria

Disease Ontology Definition:n_a

Synonyms: Coproporphyrinogen oxidase deficiency, Hereditary coproporphyria, Hereditary coproporphyria (disorder), hereditary coproporphyria porphyria

Xenbase Genes : cpox

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007369 - hereditary coproporphyria

MIM:
MIM:121300 - COPROPORPHYRIA, HEREDITARY; HCP

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): acute porphyria (is_a)