FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
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General Information
Term X-linked congenital hemolytic anemia ID (Ontology) DOID:0111846 (Human Disease)
Definition A congenital hemolytic anemia characterized by mild congenital hemolytic anemia without morphologic red cell abnormalities that has_material_basis_in hemizygous mutation in the ATP11C gene on chromosome Xq27.1.
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 Genes
 X-linked congenital hemolytic anemia       2
 for disease ribbon | X-linked congenital hemolytic anemia       2
 model of | X-linked congenital hemolytic anemia       2
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X-linked monogenic disease
 |__X-linked recessive disease___
physical disorder                |
 |__congenital hemolytic anemia__|
hemolytic anemia                 |
 |__congenital hemolytic anemia__|
                                 X-linked congenital hemolytic anemia  2 rec.
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Is a X-linked recessive disease
congenital hemolytic anemia
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MIM:301015