OMOP Concept 4327189

Hemoglobin M disease

StandardConditionSNOMED74912001Disorder
Maps from
2
Descendants
1
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept

2 source codes normalize to Hemoglobin M disease via the OMOP "Maps to" relationship.

VocabularyCodeNameType
CIEL138940Hemoglobin M diseaseNon-standard
MeSHC581942Hemoglobin M DiseaseNon-standard

Synonyms

Alternative names recorded for Hemoglobin M disease across source vocabularies.

  • enfermedad por hemoglobina M
  • Haemoglobin M disease
  • hemoglobinopatía M hereditaria
  • Hereditary methaemoglobinuria
  • Hereditary methemoglobinaemia due to globin chain mutation
  • Hereditary methemoglobinemia due to globin chain mutation
  • Hereditary methemoglobinemia due to globin chain mutation (disorder)
  • Hereditary methemoglobinuria
  • Hereditary M haemoglobinopathy
  • Hereditary M hemoglobinopathy
  • metahemoglobinemia hereditaria debida a mutación de cadena de globina
  • metahemoglobinemia hereditaria debida a mutación de cadena de globina (trastorno)
  • metahemoglobinuria hereditaria

Where it sits in the hierarchy

Ordered by distance - 1 is a direct parent or child.

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