congenital methemoglobinemia

Preferred Label : congenital methemoglobinemia;

MeSH note : promote; also known as Blue Baby Syndrome not to be confused with blue baby due to congenital heart defects;

Is substance : O;

Details

Origin ID

C580280;

UMLS CUI

C0272087;

Currated CISMeF NLP mapping
- Congenital Methemoglobinemia [NCIt concept]
- Congenital methaemoglobinaemia [ICD-10 Sub-category (who)]
- Congenital methaemoglobinaemia [MedDRA Preferred Term]
- Congenital methaemoglobinaemia [ICD-11 Category]
- Congenital methemoglobinemia [MedDRA LLT]
- Congenital methemoglobinemia [ICD-10 Sub-category]
- Congenital methemoglobinemia (disorder) [SNOMED CT concept]
- Hereditary methemoglobinemia [ORDO Disease]
- Hereditary methemoglobinemia due to globin chain mutation (disorder) [SNOMED CT concept]
- hemoglobin m disease [SNOMED Notion]
MeSH term(s) associated for indexing
- methemoglobinemia [MeSH Descriptor]
Record concept(s)
- congenital methemoglobinemia [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital Methemoglobinemia [NCIt concept]
- Congenital methaemoglobinaemia [MedDRA Preferred Term]
- Congenital methaemoglobinaemia [ICD-10 Sub-category (who)]
- Congenital methemoglobinemia [MedDRA LLT]
- Congenital methemoglobinemia [ICD-10 Sub-category]
- Congenital methemoglobinemia (disorder) [SNOMED CT concept]
- Hereditary methemoglobinemia [ORDO Disease]

Keyword's position in hierarchy(ies) :

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