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Echinobase
Summary Literature (0)
DOID:13269 - hereditary coproporphyria

Disease Ontology Definition:n_a

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

Echinobase Genes : cpox


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), digenic disease (is_a)