OMOP Concept 24909
Hereditary spherocytosis
StandardConditionSNOMED55995005Disorder
Maps from
17
Descendants
8
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
17 source codes normalize to Hereditary spherocytosis via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 138736 | Congenital spherocytic haemolytic anaemia | Non-standard |
| CIM10 | D58.0 | Hereditary spherocytosis | Non-standard |
| ICD10 | D58.0 | Hereditary spherocytosis | Non-standard |
| ICD10CM | D58.0 | Hereditary spherocytosis | Non-standard |
| ICD10CN | D58.0 | Hereditary spherocytosis | Non-standard |
| ICD10CN | D58.000 | Hereditary spherocytosis | Non-standard |
| ICD10CN | D58.001 | Congenital hemolytic anemia (machine translation) | Non-standard |
| ICD10CN | D58.002 | Minkowski - Fall elimination syndrome (machine translation) | Non-standard |
| ICD10CN | D58.003 | No bile pigments in urine Jaundice (machine translation) | Non-standard |
| ICD10GM | D58.0 | Hereditary spherocytosis | Non-standard |
| ICD9CM | 282.0 | Hereditary spherocytosis | Non-standard |
| KCD7 | D58.0 | Hereditary spherocytosis | Non-standard |
| MeSH | D013103 | Spherocytosis, Hereditary | Non-standard |
| Nebraska Lexicon | 55995005 | Congenital spherocytic haemolytic anaemia | Non-standard |
| Read | D100.00 | Hereditary spherocytosis | Non-standard |
| Read | D100.11 | Acholuric familial jaundice | Non-standard |
| Read | D100.12 | Minkowski - Chauffard syndrome | Non-standard |
Synonyms
Alternative names recorded for Hereditary spherocytosis across source vocabularies.
- anemia hemolítica esferocítica congénita
- Congenital spherocytic haemolytic anaemia
- Congenital spherocytic hemolytic anemia
- Congenital spherocytosis
- esferocitosis congénita
- esferocitosis familiar
- esferocitosis hereditaria
- esferocitosis hereditaria (trastorno)
- Familial acholuric jaundice
- Familial spherocytosis
- Hereditary spherocytosis (disorder)
- HS - Hereditary spherocytosis
- ictericia acolúrica familiar
- Minkowsky-Chauffard syndrome
- síndrome de Minkowsky - Chauffard
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(39)Roll up to these when you need a wider cohort.
- 1Anemia due to membrane defect
- 1Autosomal hereditary disorder
- 1Erythrocyte membrane abnormality
- 1Hereditary hemolytic anemia
- 2Anemia due to intrinsic red cell abnormality
- 2Hemoglobin below reference range
- 2Hemolytic anemia
- 2Hereditary disease
- 2Hereditary red blood cell disorder
- 2Red blood cell disorder
- 3Anemia
- 3Disorder of body system
- 3Disorder of cellular component of blood
- 3Genetic disease
- 3Hemoglobin level outside reference range
- 3Hemolytic disorder
- 3Hereditary disorder of cellular element of blood
- 3Measurement finding below reference range
- 3Red blood cell count below reference range
- 4Cytopenia
- 4Disease
- 4Finding of blood, lymphatics and immune system
- 4Hematology test outside reference range
- 4Hemoglobin finding
- 4Hemolysis
Narrower concepts
(8)Included automatically when you query with descendants.
- 1Hereditary spherocytosis due to beta spectrin defect
- 1Hereditary spherocytosis due to deficiency of protein 4.2
- 1Hereditary spherocytosis due to spectrin deficiency
- 2Hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin
- 2Mild hereditary spherocytosis due to spectrin deficiency
- 2Severe hereditary spherocytosis due to spectrin deficiency
- 3Mild hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin
- 3Severe hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin
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