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

Disease References using Mouse Models (1)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.12
The Jackson Laboratory