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DO Term : X-linked congenital hemolytic anemia [DOID:0111846] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  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.
  • synonyms:
  • 301015,
  • OMIM:301015
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents





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