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DO Term : autosomal recessive pyridoxine-refractory sideroblastic anemia 2 [DOID:0060065] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A sideroblastic anemia that is characterized by microcytic hypochromic anemia and iron overload, and has_material_basis_in autosomal recessive inheritance of mutation in the SLC25A38 gene.

synonyms:
205950,
pyridoxine-refractory autosomal recessive sideroblastic anemia,
OMIM:205950,
autosomal recessive pyridoxine-refractory sideroblastic anaemia 2,
pyridoxine-refractory autosomal recessive sideroblastic anaemia

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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