ORPHA:98455
Alpha granule disease
- 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 | Alpha granule disease | |
| fr | Anomalie des granules alpha | Maladie du pool vide alpha |
| de | Alpha-Granula-Defekt der Thrombozyten | |
| es | Enfermedad de gránulos alfa | |
| it | Malattia dei granuli alfa | |
| nl | Alfa-granuleziekte | |
| pt | Doença dos granulos alfa | |
| pl | Choroba ziarnistości alfa | |
| cs | Poruchy alfa granul | |
| uk | Альфа-гранулематоз | |
| zh | 阿尔法颗粒病 | |
| tr | Alfa granül hastalığı |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | 3B62.00 | E | specific | validated |
| MONDO | 0020117 | E | validated | |
| UMLS | C5681720 | 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:220452Isolated hereditary giant platelet 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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/98455
- This record as JSON: /data/d/98455.json