Search Ontology:
Human Disease

hereditary coproporphyria

Term ID
DOID:13269
Synonyms
  • Coproporphyrinogen oxidase deficiency
  • hereditary coproporphyria porphyria
Definition
References
  • GARD:6619
  • ICD10CM:E80.29
  • MESH:D046349
  • MIM:121300
  • NCI:C84759
  • SNOMEDCT_US_2023_03_01:7425008
  • UMLS_CUI:C0162531
Ontology
Human Disease   ( DOID:13269 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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