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Disease Ontology Browser
autosomal recessive pyridoxine-refractory sideroblastic anemia 2 (DOID:0060065)
Alliance: disease page
Synonyms: autosomal recessive pyridoxine-refractory sideroblastic anaemia 2; pyridoxine-refractory autosomal recessive sideroblastic anaemia; pyridoxine-refractory autosomal recessive sideroblastic anemia
Alt IDs: OMIM:205950
Definition: 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.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory