Autosomal Dominant Secondary Polycythemia

Alias:
Autosomal Dominant Secondary Erythrocytosis
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Autosomal Dominant Secondary Polycythemia, also known as autosomal dominant secondary erythrocytosis, is related to duodenal somatostatinoma and erythrocytosis, familial, 4. An important gene associated with Autosomal Dominant Secondary Polycythemia is EGLN1 (Egl-9 Family Hypoxia Inducible Factor 1), and among its related pathways/superpathways are Nuclear events mediated by NFE2L2 and Cellular responses to stimuli. Related phenotypes are Increased shRNA abundance (Z-score > 2) and muscle
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Newborn
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6
55
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Medical Symptom

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Description
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Gene & Mutation

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Disease Model

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MGI
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References Literature

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