ORPHA:98372
Hemolytic anemia due to a disorder of glycolytic enzymes
- Type
- Category
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Hemolytic anemia due to a disorder of glycolytic enzymes | |
| fr | Anémie hémolytique par anomalie des enzymes glycolytiques | |
| de | Hämolytische Anämie infolge einer Störung der glykolytischen Enzyme | |
| es | Anemia hemolítica por anomalías de las enzimas glicolíticas | |
| it | Anemia emolitica da difetti degli enzimi glicolitici | |
| nl | Hemolytische anemie als gevolg van een stoornis van glycolytische enzymen | |
| pt | Doença glicolítica | |
| pl | Niedokrwistość hemolityczna z powodu zaburzeń enzymów glikolitycznych | |
| cs | Hemolytická anémie způsobená poruchou enzymů glykolýzy | |
| uk | Гемолітична анемія внаслідок порушення гліколітичних ферментів | |
| zh | 糖酵解酶异常所致溶血性贫血 | |
| tr | Glikolitik enzim bozukluğuna bağlı hemolitik anemi |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | D55.2 | E | specific | validated |
| ICD-11 | 3A10.Y | NTBT | index | validated |
| UMLS | C5681713 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:98369Rare constitutional hemolytic anemia due to an enzyme disorder
rare genetic diseases; rare hematological diseases
Children (9):
- ORPHA:466026Class I glucose-6-phosphate dehydrogenase deficiency
- ORPHA:57Glycogen storage disease due to aldolase A deficiency
- ORPHA:371Glycogen storage disease due to muscle phosphofructokinase deficiency
- ORPHA:713Glycogen storage disease due to phosphoglycerate kinase 1 deficiency
- ORPHA:714Hemolytic anemia due to diphosphoglycerate mutase deficiency
- ORPHA:712Hemolytic anemia due to glucophosphate isomerase deficiency
- ORPHA:766Hemolytic anemia due to red cell pyruvate kinase deficiency
- ORPHA:90031Non-spherocytic hemolytic anemia due to hexokinase deficiency
- ORPHA:868Triose phosphate-isomerase deficiency
Codes that Orphanet moved or referred to this one:
- ORPHA:248305OBSOLETE: Hemolytic anemia due to glyceraldehyde-3-phosphate dehydrogenase deficiency referred to · inactive
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/98372
- This record as JSON: /data/d/98372.json