White platelet syndrome
- Type
- Disease
- Group
- Disorder
- Inheritance
- Autosomal dominant
- Age of onset
- Childhood, Infancy
- Status
- active
White platelet syndrome (WPS) is a platelet granule disorder characterized by thrombocytopenia, increased mean platelet volumes, decreased platelet responsiveness to aggregating agents, and significant defects in platelet ultrastructural morphology leading to prolonged bleeding times and bleeding.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | White platelet syndrome | |
| fr | Thrombocytopénie de White | |
| de | White-platelet-Syndrom | |
| es | Síndrome de las plaquetas de White | |
| it | Sindrome delle piastrine bianche | |
| nl | White-bloedplaatjessyndroom | |
| pt | Síndrome das plaquetas White | |
| pl | Zespół białych płytek | |
| cs | Porucha trombocytů, Whitové typ | Whitové trombocytopenie |
| uk | Синдром білих тромбоцитів | |
| zh | 白血小板综合征 | |
| tr | Beyaz trombosit sendromu |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | D69.1 | NTBT | attributed | validated |
| ICD-11 | 3B62.0Y | NTBT | attributed | validated |
| MONDO | 0018269 | E | validated | |
| MeSH | C536702 | E | validated | |
| UMLS | C2931293 | E | validated | |
| GARD | 9282 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:98455Alpha granule disease
rare genetic diseases; rare hematological diseases
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
2 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Cases/families | 1 families | Worldwide | Family(ies) | Validated | 15203719[PMID] | |
| Point prevalence | <1 / 1 000 000 | — | Worldwide | Class only | Validated | ORPHANET |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/370131
- This record as JSON: /data/d/370131.json