FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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Term Heinz body anemia ID (Ontology) DOID:0111363 (Human Disease)
Definition A congenital nonspherocytic hemolytic anemia characterized by nonspherocytic hemolytic anemia of Dacie type I with Heinz bodies seen in erythrocytes after splenectomy that has_material_basis_in heterozygous mutation in the HBA1, HBA2 or HBB genes on chromosome 11p15.4, 16p13.3, and 16p13.3, respectively.
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 Genes
 Heinz body anemia       1
 for disease ribbon | Heinz body anemia       1
 model of | Heinz body anemia       1
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autosomal genetic disease
 |__autosomal dominant disease__________________
congenital hemolytic anemia                     |
 |__congenital nonspherocytic hemolytic anemia__|
                                                Heinz body anemia  1 rec.
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Is a autosomal dominant disease
congenital nonspherocytic hemolytic anemia
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GARD:10718
MIM:140700