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Metadata
ID	DOID:0080343
Name	autosomal recessive pyridoxine-refractory sideroblastic anemia 3
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
Xrefs	MIM:616860
Parent Relationships	is_a sideroblastic anemia is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance