coproporphyria

Preferred Label : coproporphyria;

MeSH note : split;

MeSH synonym : porphyria hepatica II; porphyria hepatica, coproporphyria; hereditary coproporphyria porphyria;

Details

Origin ID

C535469;

UMLS CUI

C0342856;

Automatic exact mappings (from CISMeF team)
- Coproporphyria [PASCAL descriptor]
- Hereditary coproporphyria (disorder) [SNOMED CT concept]
- coproporphyrinogen oxidase [ORDO Gene]
- coproporphyrinogen oxidase [HGNC gene]
- hereditary coproporphyria [DO Concept]
CISMeF manual mappings
- Coproporphyria (disorder) [SNOMED CT concept]
MeSH term(s) associated for indexing
- coproporphyria, hereditary [MeSH Descriptor]
Record concept(s)
- coproporphyria [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Coproporphyria (disorder) [SNOMED CT concept]

Keyword's position in hierarchy(ies) :

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