OMOP Concept 434156
Congenital anemia
StandardConditionSNOMED63565007Disorder
Maps from
12
Descendants
68
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
12 source codes normalize to Congenital anemia via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 144271 | Congenital anaemia | Non-standard |
| CIM10 | P61.4 | Other congenital anaemias, not elsewhere classified | Non-standard |
| ICD10 | P61.4 | Other congenital anaemias, not elsewhere classified | Non-standard |
| ICD10CM | P61.4 | Other congenital anemias, not elsewhere classified | Non-standard |
| ICD10CN | P61.4 | Other congenital anaemias, not elsewhere classified | Non-standard |
| ICD10CN | P61.400 | Other congenital anaemias, not elsewhere classified | Non-standard |
| ICD10GM | P61.4 | Other congenital anaemias, not elsewhere classified | Non-standard |
| ICD9CM | 776.5 | Congenital anemia | Non-standard |
| KCD7 | P61.4 | Other congenital anaemias, NEC | Non-standard |
| Nebraska Lexicon | 63565007 | Congenital anaemia | Non-standard |
| Read | Q455.00 | Congenital anaemia | Non-standard |
| Read | Qyu5C00 | [X]Other congenital anaemias, not elsewhere classified | Non-standard |
Synonyms
Alternative names recorded for Congenital anemia across source vocabularies.
- anemia congénita
- anemia congénita (trastorno)
- Congenital anaemia
- Congenital anemia (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(24)Roll up to these when you need a wider cohort.
- 1Anemia
- 1Congenital disease
- 1Hemoglobin below reference range
- 1Red blood cell count below reference range
- 2Cytopenia
- 2Disorder of cellular component of blood
- 2Disorder of fetus and/or newborn
- 2Hemoglobin level outside reference range
- 2Measurement finding below reference range
- 2Red blood cell count outside reference range
- 3Blood cell count outside reference range
- 3Disease
- 3Finding of blood, lymphatics and immune system
- 3Hematology test outside reference range
- 3Hemoglobin finding
- 3Measurement finding outside reference range
- 3Red blood cell count - finding
- 4Clinical finding
- 4Hematopoietic system finding
- 4Measurement finding
- 4Protein level - finding
- 5Evaluation finding
- 5Finding of substance level
- 6Procedure related finding
Narrower concepts
(68)Included automatically when you query with descendants.
- 1Alpha plus thalassemia deletion type
- 1Alpha plus thalassemia non deletion type
- 1Alpha-thalassemia intellectual disability syndrome linked to chromosome 16
- 1Alpha thalassemia X-linked intellectual disability syndrome
- 1Congenital dyserythropoietic anemia
- 1Congenital hemolytic anemia
- 1Congenital hemolytic uremic syndrome
- 1Congenital hypoplastic anemia
- 1Congenital sideroblastic anemia, B-cell immunodeficiency, periodic fever, developmental delay syndrome
- 1Congenital transferrin deficiency
- 1Constitutional aplastic anemia
- 1Epsilon gamma delta beta0 thalassemia
- 1Gamma delta beta thalassemia
- 1Ghosal hematodiaphyseal dysplasia
- 1Hemoglobin Bart's hydrops syndrome
- 1HNSHA due to hexokinase deficiency
- 1HNSHA due to NADH diaphorase deficiency
- 1Late anemia of newborn
- 1Lethal hemolytic anemia and genital anomaly syndrome
- 1Megaloblastic anemia due to inborn errors of metabolism
- 1Physiological anemia of infancy
- 1Severe combined immunodeficiency with reticular dysgenesis
- 1Thalassemia in mother complicating childbirth
- 1Thalassemia in mother complicating pregnancy
- 1Unstable hemoglobin disease
- 1X chromosome-linked sideroblastic anemia
- 2Aase syndrome
- 2AMeD syndrome
- 2Congenital atransferrinemia
- 2Congenital dyserythropoietic anemia, type I
- 2Congenital dyserythropoietic anemia, type II
- 2Congenital dyserythropoietic anemia, type III
- 2Congenital dyserythropoietic anemia type IV
- 2Congenital megaloblastic anemia due to transcobalamin II deficiency
- 2Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism
- 2Constitutional aplastic anemia with malformation
- 2Familial megaloblastic anemia
- 2Fanconi's anemia
- 2Hereditary elliptocytosis
- 2Hereditary isolated aplastic anemia
- 2Juvenile type megaloblastic anemia
- 2Late anemia of newborn due to isoimmunization
- 2Majeed syndrome
- 2Megaloblastic anemia due to congenital deficiency of intrinsic factor
- 2Megaloblastic anemia due to error of cobalamin metabolism
- 2Megaloblastic anemia due to error of folate metabolism
- 2Pancreatic insufficiency, dyserythropoietic anemia, calvarial hyperostosis syndrome
- 2Pancytopenia with developmental delay syndrome
- 2Revesz syndrome
- 2Thiamine-responsive megaloblastic anemia
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