Disease #04474 (FGFR1OP (myeloproliferative disorder (FGFR-1OP)), OMIM:605392)
| Official abbreviation |
FGFR1OP |
| Name |
myeloproliferative disorder (FGFR-1OP) |
| OMIM ID |
605392 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
FGFR1OP |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-09-23 10:25:22 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|