FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term hereditary coproporphyria ID (Ontology) DOID:13269 (Human Disease)
Definition
Also Known As "Coproporphyrinogen oxidase deficiency" ; "hereditary coproporphyria porphyria"
Comment
Links to External Ontologies
DO.org
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 Genes
 hereditary coproporphyria       1
 for disease ribbon | hereditary coproporphyria       1
 model of | hereditary coproporphyria       1
Spanning Tree (Parents/Children)
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polygenic disease
 |__digenic disease__
porphyria            |
 |__acute porphyria__|
                     hereditary coproporphyria  1 rec.
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Is a digenic disease
acute porphyria
Part of
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Synonyms
  • "Coproporphyrinogen oxidase deficiency" EXACT
    "hereditary coproporphyria porphyria" EXACT
Secondary IDs
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GARD:6619
ICD10CM:E80.29
MESH:D046349
MIM:121300
NCI:C84759
SNOMEDCT_US_2023_03_01:7425008
UMLS_CUI:C0162531