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
|