OMOP Concept 4327189
Hemoglobin M disease
StandardConditionSNOMED74912001Disorder
Maps from
2
Descendants
1
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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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.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 138940 | Hemoglobin M disease | Non-standard |
| MeSH | C581942 | Hemoglobin M Disease | Non-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.
Broader concepts
(18)Roll up to these when you need a wider cohort.
- 1Congenital methemoglobinemia
- 1Hereditary hemoglobinopathy due to globin chain mutation
- 2Congenital disease
- 2Hereditary hemoglobinopathy
- 2Hereditary red blood cell disorder
- 2Methemoglobinemia
- 3Fetal and/or neonatal disorder
- 3Hemoglobinopathy
- 3Hereditary disorder of cellular element of blood
- 3Red blood cell disorder
- 4Disease
- 4Disorder of body system
- 4Disorder of cellular component of blood
- 4Hereditary disorder by system
- 5Clinical finding
- 5Finding of blood, lymphatics and immune system
- 5Hereditary disease
- 6Genetic disease
Narrower concepts
(1)Included automatically when you query with descendants.
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