FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
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General Information
Term congenital nonspherocytic hemolytic anemia 5 ID (Ontology) DOID:0051006 (Human Disease)
Definition A congenital nonspherocytic hemolytic anemia that has_material_basis_in homozygous or compound heterozygous mutation in the HK1 gene, which encodes a form of hexokinase, on chromosome 10q22.
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 congenital nonspherocytic hemolytic anemia 5       1
 for disease ribbon | congenital nonspherocytic hemolytic anemia 5       1
 model of | congenital nonspherocytic hemolytic anemia 5       1
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autosomal genetic disease
 |__autosomal recessive disease_________________
congenital hemolytic anemia                     |
 |__congenital nonspherocytic hemolytic anemia__|
                                                congenital nonspherocytic hemolytic anemia 5  1 rec.
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Is a autosomal recessive disease
congenital nonspherocytic hemolytic anemia
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MIM:235700