Disease #02406 (THCYT2 (thrombocythemia, type 2), OMIM:601977)
| Official abbreviation |
THCYT2 |
| Name |
thrombocythemia, type 2 |
| OMIM ID |
601977 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant, Somatic mutation |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
MPL |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2023-09-01 13:02:12 +02:00 (CEST) |
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|