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) |
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