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DO Term : Fanconi anemia complementation group E [DOID:0111084] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A Fanconi anemia that has_material_basis_in homozygous mutation in the FANCE gene on chromosome 6p22-p21.
  • synonyms:
  • OMIM:600901,
  • FANCE,
  • 600901,
  • FACE
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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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