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DOID:0060065 - autosomal recessive pyridoxine-refractory sideroblastic anemia 2
Disease Ontology 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.
Synonyms: autosomal recessive pyridoxine-refractory sideroblastic anaemia 2, pyridoxine-refractory autosomal recessive sideroblastic anaemia, pyridoxine-refractory autosomal recessive sideroblastic anemia,
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MONDO:0008785 - sideroblastic anemia 2 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee