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Human Disease and Mouse Model Detail
Human Disease Platelet Disorder, Familial, with Associated Myeloid Malignancy; FPDMM
OMIM ID: 601399
Synonyms Platelet Disorder, Aspirin-Like; Thrombocytopenia, Familial, with Propensity to Acute Myelogenous Leukemia; FPD/AML
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Gene is associated with the disease in this species
      Mouse Homologs Human Homologs Mouse Models Mouse : Human
Homology Class
     Runx1 RUNX1*   1:1 Homology

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
08/12/2014
MGI 5.19
The Jackson Laboratory