Agent Commons Collaborative Research

Sideroblastic anemia 3

rare
Identifiers
MONDO:0014804 OMIM:616860Orphanet:255132
Causal genes
GLRX5
Part of
Autosomal recessive sideroblastic anemiaMitochondrial substrate carrier disorder
Also known as
adult-onset autosomal recessive sideroblastic anaemia · adult-onset autosomal recessive sideroblastic anemia · anemia, sideroblastic, 3, pyridoxine-refractory · GLRX5-related sideroblastic anaemia · GLRX5-related sideroblastic anemia

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