OMOP Concept 4214408
Hereditary disorder of cellular element of blood
StandardConditionSNOMED414393003Disorder
Maps from
1
Descendants
324
Valid from
31 Jan 2005
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Hereditary disorder of cellular element of blood via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| UK Biobank | 6-1451 | hereditary/genetic haematological disorder | Non-standard |
Synonyms
Alternative names recorded for Hereditary disorder of cellular element of blood across source vocabularies.
- Hereditary disorder of cellular element of blood (disorder)
- trastorno hereditario de componente celular sanguíneo
- trastorno hereditario de componente celular sanguíneo (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(8)Roll up to these when you need a wider cohort.
Narrower concepts
(324)Included automatically when you query with descendants.
- 1Aase syndrome
- 1CAD-CDG - carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase congenital disorder of glycosylation
- 1Central nervous system calcification, deafness, tubular acidosis, anemia syndrome
- 1Congenital sideroblastic anemia, B-cell immunodeficiency, periodic fever, developmental delay syndrome
- 1Ghosal hematodiaphyseal dysplasia
- 1Hereditary red blood cell disorder
- 1Hereditary white blood cell disorder
- 1Inherited platelet disorder
- 1Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness
- 1Mitochondrial myopathy with sideroblastic anemia syndrome
- 2Adult-onset autosomal recessive sideroblastic anemia
- 2AMeD syndrome
- 2Ataxia pancytopenia syndrome
- 2Autosomal dominant secondary polycythemia
- 2Chédiak-Higashi syndrome
- 2Combined immunodeficiency, enteropathy spectrum
- 2Congenital dyserythropoietic anemia
- 2Congenital methemoglobinemia
- 2Congenital neutropenia, myelofibrosis, nephromegaly syndrome
- 2Cystic fibrosis with gastritis and megaloblastic anemia syndrome
- 2Dehydrated hereditary stomatocytosis
- 2Familial erythrocytosis
- 2Familial hemophagocytic lymphohistiocytosis
- 2Familial thrombocytosis
- 2Fanconi's anemia
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