ORPHA:26349
Protein S acquired deficiency
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Protein S acquired deficiency | |
| fr | Déficit acquis en protéine S | |
| de | Protein-S-Mangel, erworbener | |
| es | Deficiencia adquirida de proteina S | |
| it | Deficit acquisito della proteina S | |
| nl | Verworven proteïne S-deficiëntie | |
| pt | Deficiência de proteína S adquirida | |
| pl | Nabyty Niedobór białka S | |
| cs | Získaný deficit proteinu S | |
| uk | Набутий дефіцит протеїну S | |
| zh | 获得性蛋白S缺乏症 | |
| tr | Protein S edinsel yetmezliği |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | D68.8 | NTBT | attributed | validated |
| ICD-11 | 3B61.1 | NTBT | index | validated |
| MONDO | 0012868 | E | validated | |
| MONDO | 12868 | E | validated | |
| MeSH | C567077 | E | validated | |
| UMLS | C2363755 | E | validated | |
| MedDRA | 10068370 | 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:248365Rare thrombotic disorder due to an acquired coagulation factors defect
rare hematological diseases
No children.
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/26349
- This record as JSON: /data/d/26349.json