Congenital dyserythropoietic anemia, type II Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Congenital dyserythropoietic anemia type II (CDA II) is the most common form of CDA (see this term) characterized by anemia, jaundice and splenomegaly and often leading to liver iron overload and gallstones. (Orphanet Rare Disease Ontology, Orphanet_98873)
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1 genes associated with the Congenital dyserythropoietic anemia, type II phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
SEC23B Sec23 homolog B (S. cerevisiae)