MeSH Browser

MeSH Supplementary: Coproporphyria
Unique ID: C535469
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C535469
Entry Term(s): Hereditary coproporphyria porphyria; Porphyria Hepatica, Coproporphyria; Porphyria hepatica II
Heading Mapped to: *Coproporphyria, Hereditary
Frequency: 26
Note: split
Date of Entry: 2010/11/13
Revision Date: 1955/01/01

Concept UI: M0529930
Terms: Coproporphyria Preferred Term
Term UI T736162
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); Hereditary coproporphyria porphyria
Term UI T736163
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); Porphyria hepatica II
Term UI T736165
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); Porphyria Hepatica, Coproporphyria
Term UI T736164
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010)

Coproporphyria MeSH Supplementary Concept Data 2024