OBO ID: DOID:0080343 |
Term Name: | autosomal recessive pyridoxine-refractory sideroblastic anemia 3 | Search Ontology: | |
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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 | ||
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Ontology: | Human Disease ( DOID:0080343 ) |
OTHER autosomal recessive pyridoxine-refractory sideroblastic anemia 3 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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