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Disease Ontology Browser
autosomal recessive pyridoxine-refractory sideroblastic anemia 3 (DOID:0080343)
Alliance: disease page
Alt IDs: OMIM:616860
Definition: A sideroblastic anemia that is characterized by homozygous or compound heterozygous mutation in the GLRX5 gene on chromosome 14q32.


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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last database update
01/31/2023
MGI 6.22
The Jackson Laboratory