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DO Term : hereditary spherocytosis type 4 [DOID:0110919] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A hereditary spherocytosis that has_material_basis_in an autosomal dominant mutation of the SLC4A1 gene on chromosome 17q21.31.
  • synonyms:
  • HS4,
  • OMIM:612653,
  • 612653,
  • SPH4,
  • hereditary spherocytosis 4
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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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