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Human Disease

autosomal recessive pyridoxine-refractory sideroblastic anemia 3

Term ID
DOID:0080343
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 )
Relationships
is a type of
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Genes Involved
Zebrafish Models