Thalassemia

Alias:
Thalassemia Hb-S Disease Without Crisis
Sickle-Cell Thalassemia Without Crisis
Thalassemia Hb-S Disease with Crisis
Sickle-Cell Thalassemia with Crisis
Haemoglobin Thalassaemia Disorder
Hereditary Leptocytosis
Thalassaemia Syndrome
Thalassemia Variants
Thalassaemia Nos
Thalassemias
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Thalassemia, also known as sickle-cell thalassemia without crisis, is related to beta-thalassemia, dominant inclusion body type and hemoglobin e-beta-thalassemia syndrome, and has symptoms including angina pectoris, chest pain and edema. An important gene associated with Thalassemia is MIR144 (MicroRNA 144), and among its related pathways/superpathways are Golgi-to-ER retrograde transport and Binding and Uptake of Ligands by Scavenger Receptors. The drugs Peginterferon alfa-2b and Metformin have been mentioned in the context of this disorder. Affiliated tissues include bone marrow and bone, and related phenotypes are Increased shRNA abundance (Z-score > 2) and Increased shRNA abundance
Related ID:
MESH:D013789
ICD11:330259189

Basic Information

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Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Medical Symptom

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Gene & Mutation

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References Literature

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