Thrombocytopenia with Beta-Thalassemia, X-Linked (XLTT)

Alias:
Thrombocytopenia, Platelet Dysfunction, Hemolysis, and Imbalanced Globin Synthesis
Beta-Thalassemia-X-Linked Thrombocytopenia Syndrome
Xltt
X-Linked Thrombocytopenia with Beta-Thalassemia
Gata1-Related X-Linked Cytopenia
Thrombocytopenia Platelet Dysfunction Hemolysis and Imbalanced Globin Synthesis
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Thrombocytopenia with Beta-Thalassemia, X-Linked, also known as thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis, is related to thrombocytopenia 1 and thrombocytopenia, and has symptoms including petechiae of skin An important gene associated with Thrombocytopenia with Beta-Thalassemia, X-Linked is GATA1 (GATA Binding Protein 1), and among its related pathways/superpathways are Response to elevated platelet cytosolic Ca2+ and C-MYB transcription factor network. Affiliated tissues include bone marrow and bone, and related phenotypes are splenomegaly and anemia
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
XL
XLD
Unknown
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11
71
22

Medical Symptom

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Gene & Mutation

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References Literature

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