OMOP Concept 4254249
HNSHA (hereditary nonspherocytic hemolytic anemia) due to pyruvate kinase deficiency
StandardConditionSNOMED74703006Disorder
Maps from
6
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
6 source codes normalize to HNSHA (hereditary nonspherocytic hemolytic anemia) due to pyruvate kinase deficiency via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 138556 | HNSHA due to Pyruvate Kinase Deficiency | Non-standard |
| ICD10CM | D55.21 | Anemia due to pyruvate kinase deficiency | Non-standard |
| Nebraska Lexicon | 191178002 | Haemolytic anaemia due to pyruvate kinase deficiency | Non-standard |
| Nebraska Lexicon | 74703006 | Hereditary nonspherocytic hemolytic anemia due to pyruvate kinase deficiency | Non-standard |
| OXMIS | 2823PK | ANAEMIA PYRUVATE-KINASE DEFICIENCY | Non-standard |
| Read | D103100 | Haemolytic anaemia due to pyruvate kinase deficiency | Non-standard |
Synonyms
Alternative names recorded for HNSHA (hereditary nonspherocytic hemolytic anemia) due to pyruvate kinase deficiency across source vocabularies.
- anemia hemolítica no esferocítica hereditaria debida a deficiencia de piruvato quinasa
- anemia hemolítica no esferocítica hereditaria debida a deficiencia de piruvato quinasa (trastorno)
- anemia hemolítica no esferocítica hereditaria por deficiencia de piruvato cinasa
- anemia hemolítica no esferocítica hereditaria por deficiencia de piruvato quinasa
- anemia por deficiencia de piruvato cinasa
- anemia por deficiencia de piruvato quinasa
- anemia por deficiencia de PK
- Hereditary nonspherocytic haemolytic anaemia due to pyruvate kinase deficiency
- Hereditary nonspherocytic hemolytic anemia due to pyruvate kinase deficiency
- Hereditary nonspherocytic hemolytic anemia due to pyruvate kinase deficiency (disorder)
- HNSHA (hereditary nonspherocytic haemolytic anaemia) due to pyruvate kinase deficiency
- PK (pyruvate kinase) deficiency haemolytic anaemia
- PK (pyruvate kinase) deficiency hemolytic anemia
- Pyruvate kinase deficiency anaemia
- Pyruvate kinase deficiency anemia
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(41)Roll up to these when you need a wider cohort.
- 1Anemia due to enzyme deficiency
- 1Autosomal recessive hereditary disorder
- 1Hereditary nonspherocytic hemolytic anemia
- 2Anemia due to enzymopathy
- 2Autosomal hereditary disorder
- 2Hemolytic anemia
- 2Hereditary hemolytic anemia
- 3Anemia
- 3Anemia due to metabolic disorder
- 3Hemoglobin below reference range
- 3Hemolytic disorder
- 3Hereditary disease
- 3Hereditary red blood cell disorder
- 3Red blood cell count below reference range
- 4Cytopenia
- 4Disorder of cellular component of blood
- 4Genetic disease
- 4Hemoglobin level outside reference range
- 4Hemolysis
- 4Hereditary disorder of cellular element of blood
- 4Measurement finding below reference range
- 4Red blood cell count outside reference range
- 4Red blood cell disorder
- 5Blood cell count outside reference range
- 5Disease
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