Disease #01578 (THCYT1 (thrombocythemia, type 1), OMIM:187950)
| Official abbreviation |
THCYT1 |
| Name |
thrombocythemia, type 1 |
| OMIM ID |
187950 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
2 |
| Associated with 3 genes |
CALR, SH2B3, THPO |
| Associated tissues |
- |
| Disease features |
autosomal dominant |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2023-09-01 13:05:31 +02:00 (CEST) |
Individuals
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