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Query OMIM entry list
601399
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PLATELET DISORDER, FAMILIAL, WITH ASSOCIATED MYELOID MALIGNANCY
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Neoplasms
Neoplasms by Histologic Type
Leukemia
Leukemia, Myeloid
Leukemia, Myeloid, Acute
Leukemia, Erythroblastic, Acute
Leukemia, Monocytic, Acute
Lymphoma
Lymphoma, Non-Hodgkin
Neoplasms, Germ Cell and Embryonal
Neuroectodermal Tumors
Neoplasms, Neuroepithelial
Neuroectodermal Tumors, Primitive
Neuroectodermal Tumors, Primitive, Peripheral
Neuroblastoma
Neoplasms, Glandular and Epithelial
Neoplasms, Neuroepithelial
Neuroectodermal Tumors, Primitive
Neuroectodermal Tumors, Primitive, Peripheral
Neuroblastoma
Neoplasms, Nerve Tissue
Neuroectodermal Tumors
Neoplasms, Neuroepithelial
Neuroectodermal Tumors, Primitive
Neuroectodermal Tumors, Primitive, Peripheral
Neuroblastoma
Neoplastic Syndromes, Hereditary
Hemic and Lymphatic Diseases
Hematologic Diseases
Blood Platelet Disorders
Thrombocytopenia
Bone Marrow Diseases
Myelodysplastic Syndromes
Myeloproliferative Disorders
Leukemia, Erythroblastic, Acute
Hemorrhagic Disorders
Lymphatic Diseases
Lymphoproliferative Disorders
Lymphoma
Lymphoma, Non-Hodgkin
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Neoplastic Syndromes, Hereditary
Immune System Diseases
Immunoproliferative Disorders
Lymphoproliferative Disorders
Lymphoma
Lymphoma, Non-Hodgkin
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Trisomy
Chromosome Duplication
Trisomy
Disease Attributes
Acute Disease
Disease Progression
Disease Susceptibility
Genetic Predisposition to Disease
Hemorrhage
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