ORPHA:98370
Hemolytic anemia due to hexose monophosphate shunt and glutathione metabolism anomalies
- 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.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Hemolytic anemia due to hexose monophosphate shunt and glutathione metabolism anomalies | |
| fr | Anémie hémolytique due à une anomalie du métabolisme du glutathion et du shunt hexose monophosphate | |
| de | Hämolytische Anämie durch Hexosemonophosphat-Shunt/Glutathion-Stoffwechselstörung | |
| es | Anemia hemolítica por anomalías en el metabolismo de la vías de la hexosa monofosfato y glutation | |
| it | Anemia emolitica da anomalie del metabolismo del glutatione e shunt dell'esoso monofosfato | |
| nl | Hemolytische anemie als gevolg van hexosemonofosfaatshunt en glutathionmetabolismeanomalieën | |
| pt | Anemia hemolítica por anomalias do shunt hexose monofosfato e metabolismo da glutationa | |
| pl | Niedokrwistość hemolityczna z powodu minięcia monofosforanu heksozy i zaburzeń metabolizmu glutationu | |
| cs | Hemolytická anémie způsobená zkratem hexoso-monofosfátového cyklu a anomáliemi metabolismu glutathionu | |
| uk | Гемолітична анемія внаслідок гексозомонофосфатного шунта та аномалій метаболізму глутатіону | |
| zh | 磷酸己糖分流和谷胱甘肽代谢异常所致溶血性贫血 | |
| tr | Heksoz tekfosfatlı döngüye bağlı hemolitik anemi ve glutatyon metabolizması anomalileri |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | 3A10.0 | E | specific | validated |
| UMLS | C5681714 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
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
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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/98370
- This record as JSON: /data/d/98370.json