FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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Term congenital nonspherocytic hemolytic anemia 1 ID (Ontology) DOID:0051003 (Human Disease)
Definition A congenital nonspherocytic hemolytic anemia that has_material_basis_in mutation in the G6PD gene on chromosome Xq28, and is the most common genetic form of chronic and drug-, food-, or infection-induced hemolytic anemia.
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 congenital nonspherocytic hemolytic anemia 1       2
 for disease ribbon | congenital nonspherocytic hemolytic anemia 1       2
 model of | congenital nonspherocytic hemolytic anemia 1       2
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monogenic disease
 |__X-linked monogenic disease__________________
congenital hemolytic anemia                     |
 |__congenital nonspherocytic hemolytic anemia__|
                                                congenital nonspherocytic hemolytic anemia 1  2 rec.
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Is a X-linked monogenic disease
congenital nonspherocytic hemolytic anemia
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MIM:300908