hemoglobin M disease

Preferred Label : hemoglobin M disease;

MeSH note : promote; specific types of Hemoglobin M disease (methemoglobinemia due to hemoglobin M beta types, or alpha types) represented by several scr;

Details

Origin ID

C581942;

UMLS CUI

C3665425;

Automatic exact mappings (from CISMeF team)
- Hemoglobin M disease [ORDO Disease]
- Hereditary methemoglobinemia due to globin chain mutation (disorder) [SNOMED CT concept]
- hemoglobin m disease [SNOMED Notion]
MeSH term(s) associated for indexing
- hemoglobin m [MeSH Descriptor]
- methemoglobinemia [MeSH Descriptor]
Record concept(s)
- hemoglobin M disease [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hereditary methemoglobinemia due to globin chain mutation (disorder) [SNOMED CT concept]
- hemoglobin m disease [SNOMED Notion]

Keyword's position in hierarchy(ies) :

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