Platelet Disorder, Familial, with Associated Myeloid Malignancy (FPDMM)

Alias:

Fpdmm

Familial Platelet Disorder with Associated Myeloid Malignancy

Fpd/aml

Familial Platelet Disorder with Predisposition to Acute Myelogenous Leukemia

Familial Thrombocytopenia with Propensity to Acute Myelogenous Leukemia

Familial Platelet Disorder with Predisposition to Myeloid Malignancy

Familial Platelet Disorder with Propensity to Acute Myeloid Leukemia

Fps/aml

Hereditary Thrombocytopenia and Hematological Cancer Predisposition Syndrome Associated with Runx1

Thrombocytopenia, Familial, with Propensity to Acute Myelogenous Leukemia

Platelet Disorder, Aspirin-Like

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Platelet Disorder, Familial, with Associated Myeloid Malignancy, also known as fpdmm, is related to qualitative platelet defect and chronic myelomonocytic leukemia. An important gene associated with Platelet Disorder, Familial, with Associated Myeloid Malignancy is RUNX1 (RUNX Family Transcription Factor 1). Affiliated tissues include myeloid and bone marrow, and related phenotypes are prolonged bleeding time and impaired platelet aggregation

Related ID：

MALACARDS：PLT019

OMIM：601399