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Human Disease
autosomal recessive pyridoxine-refractory sideroblastic anemia 3
- Term ID
- DOID:0080343
- Synonyms
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- Definition
- A sideroblastic anemia that is characterized by homozygous or compound heterozygous mutation in the GLRX5 gene on chromosome 14q32. https://www.omim.org/entry/616860?search=616860&highlight=616860
- References
- Ontology
- Human Disease ( DOID:0080343 )
- is a type of
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