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Coproporphyria, Hereditary

Disease ID: disease_node_11282

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Dbxref	GARD:6619, ICD10CM:E80.29, MESH:D046349, MIM:121300, NCI:C84759, SNOMEDCT_US_2023_03_01:7425008, UMLS_CUI:C0162531
Subclassof	DOID_3133, DOID_0080578
Data Source	DOID, MESH
Synonyms	Coproporphyrinogen oxidase deficiency, hereditary coproporphyria porphyria
Mesh Id	D046349
Mesh Label	Coproporphyria, Hereditary
Mesh Subclassof	D017094
Doid Label	hereditary coproporphyria
Doid Description	OMIM mapping confirmed by DO. [SN].
Has Material Basis In	GENO_0000930
Disease Node Id	disease_node_11282
Doid Id	DOID_13269
Label	Coproporphyria, Hereditary

Outgoing r'ship SUBCLASS_OF to/from Porphyrias, Hepatic(ID:disease_node_9037) (Disease)
Outgoing r'ship SUBCLASS_OF to/from Digenic Disease(ID:disease_node_13627) (Disease)

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