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DO Term : sideroblastic anemia 5 [DOID:0061007] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A sideroblastic anemia that is characterized by abnormal iron accumulation in the mitochondria or erythroid cells that has_material_basis_in compound heterozygous mutation in the HSCB gene on chromosome 22q12.
  • synonyms:
  • 619523,
  • SIDBA5,
  • OMIM:619523
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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