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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