ORPHA:93573
Thrombotic microangiopathy
Synonyms: TMA
- Type
- Clinical group
- 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 | Thrombotic microangiopathy | TMA |
| fr | Microangiopathie thrombotique | MAT |
| de | Mikroangiopathie, thrombotische | = en |
| es | Microangiopatía trombótica | |
| it | Microangiopatia trombotica | = en |
| nl | Trombotische microangiopathie | = en |
| pt | Microangiopatia trombótica | |
| pl | Mikroangiopatia zakrzepowa | = en |
| cs | Trombotické mikroangiopatie | = en |
| uk | Тромботична мікроангіопатія | = en |
| zh | 血栓性微血管病 | = en |
| tr | Trombotik mikroanjiyopati | = en |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0019737 | E | validated | |
| MeSH | D057049 | E | validated | |
| UMLS | C2717961 | E | validated | |
| MedDRA | 10043645 | 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:93626Rare renal disease
rare renal 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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/93573
- This record as JSON: /data/d/93573.json