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DO Term : congenital nonspherocytic hemolytic anemia 5 [DOID:0051006] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  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.
  • synonyms:
  • OMIM:235700,
  • 235700
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Disease

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Ontology

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Ontology Term --> Direct parents





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