OMOP Concept 40599994
X chromosome-linked sideroblastic anemia
StandardConditionSNOMED48983004Disorder
Maps from
12
Descendants
3
Valid from
31 Jul 2018
Valid to
31 Dec 2099
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Source codes that map to this concept
12 source codes normalize to X chromosome-linked sideroblastic anemia via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 138738 | Hereditary sideroblastic anaemia | Non-standard |
| CIM10 | D64.0 | Hereditary sideroblastic anaemia | Non-standard |
| ICD10 | D64.0 | Hereditary sideroblastic anaemia | Non-standard |
| ICD10CM | D64.0 | Hereditary sideroblastic anemia | Non-standard |
| ICD10CN | D64.0 | Hereditary sideroblastic anaemia | Non-standard |
| ICD10CN | D64.000 | Hereditary sideroblastic anaemia | Non-standard |
| ICD10CN | D64.001 | Hypopigmented sex-linked sideroblastic anemia (machine translation) | Non-standard |
| ICD10GM | D64.0 | Hereditary sideroblastic anaemia | Non-standard |
| KCD7 | D64.0 | Hereditary sideroblastic anaemia | Non-standard |
| MeSH | C536761 | X-linked sideroblastic anemia | Non-standard |
| Nebraska Lexicon | 48983004 | X-linked sideroblastic anaemia | Non-standard |
| Read | D210000 | Congenital sideroblastic anaemia | Non-standard |
Synonyms
Alternative names recorded for X chromosome-linked sideroblastic anemia across source vocabularies.
- anemia sideroblástica ligada al cromosoma X
- anemia sideroblástica ligada al cromosoma X (trastorno)
- X chromosome-linked sideroblastic anaemia
- X chromosome-linked sideroblastic anemia (disorder)
- X-linked sideroblastic anaemia
- X-linked sideroblastic anemia
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(40)Roll up to these when you need a wider cohort.
- 1Congenital anemia
- 1Hereditary red blood cell disorder
- 1Inherited disorder of porphyrin metabolism
- 1Sideroblastic anemia
- 1X-linked recessive hereditary disease
- 2Anemia
- 2Congenital disease
- 2Disorder of porphyrin metabolism
- 2Hemoglobin below reference range
- 2Hereditary disorder of cellular element of blood
- 2Hereditary metabolic disease
- 2Red blood cell count below reference range
- 2Red blood cell disorder
- 2X-linked hereditary disease
- 3Cytopenia
- 3Disorder of body system
- 3Disorder of cellular component of blood
- 3Disorder of fetus and/or newborn
- 3Hemoglobin level outside reference range
- 3Hereditary disease
- 3Hereditary disorder by system
- 3Measurement finding below reference range
- 3Metabolic disease
- 3Red blood cell count outside reference range
- 3Sex-linked hereditary disorder
Narrower concepts
(3)Included automatically when you query with descendants.
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