Pure Red-Cell Aplasia

Alias:
Pure Red Cell Aplasia
Primary Red Cell Aplasia
Red-Cell Aplasia, Pure
Red-Cell Aplasia Pure
Red Cell Hypoplasia
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Pure Red-Cell Aplasia, also known as pure red cell aplasia, is related to transient erythroblastopenia of childhood and thymoma type b. An important gene associated with Pure Red-Cell Aplasia is RPS26 (Ribosomal Protein S26), and among its related pathways/superpathways are Metabolism of proteins and Metabolism. The drugs Tacrolimus and Immunologic Factors 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 Negative genetic interaction between KRASG13D/+ and KRAS+/-
Related ID:
MESH:D012010
ICD11:1980066564

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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Medical Symptom

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Gene & Mutation

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MGI
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References Literature

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