Congenital Nonspherocytic Hemolytic Anemia (HNSHA)

Alias:
Anemia, Hemolytic, Congenital Nonspherocytic
Hereditary Non-Spherocytic Hemolytic Anemia
Hereditary Nonspherocytic Hemolytic Anemia
Congenital Nonspherocytic Hemolytic Anaemia
Hereditary Nonspherocytic Hemolytic Anaemia
Hnsha
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Congenital Nonspherocytic Hemolytic Anemia, also known as anemia, hemolytic, congenital nonspherocytic, is related to triosephosphate isomerase deficiency and glucosephosphate dehydrogenase deficiency. An important gene associated with Congenital Nonspherocytic Hemolytic Anemia is GPI (Glucose-6-Phosphate Isomerase), and among its related pathways/superpathways are Glycosaminoglycan metabolism and Collagen chain trimerization. The drugs Benzocaine and Mitapivat have been mentioned in the context of this disorder. Affiliated tissues include skin and myeloid, and related phenotypes are homeostasis/metabolism and growth/size/body region
Related ID:
MESH:D000746

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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16
124
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Medical Symptom

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Description
HPO Frequency
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Gene & Mutation

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Related Drugs

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Disease Model

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MGI
Related Gene
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Publications
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References Literature

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