OBO ID: DOID:0080343
Term Name: autosomal recessive pyridoxine-refractory sideroblastic anemia 3 Search Ontology:
Synonyms:
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)
OTHER autosomal recessive pyridoxine-refractory sideroblastic anemia 3 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
GLRX5 Anemia, sideroblastic, 3, pyridoxine-refractory 616860
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None