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Disease Ontology Browser
hereditary coproporphyria (DOID:13269)
Alliance: disease page
Synonyms: Coproporphyrinogen oxidase deficiency; hereditary coproporphyria porphyria
Alt IDs: OMIM:121300, ICD10CM:E80.29, MESH:D046349, NCI:C84759, UMLS_CUI:C0162531

Disease References using Mouse Models (2)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory