Beta thalassemia intermedia Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Beta-thalassemia (BT) intermedia is a form of BT (see this term) characterized by mild to moderate anemia which does not or only occasionally requires transfusion. (Orphanet Rare Disease Ontology, Orphanet_231222)
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1 genes associated with the Beta thalassemia intermedia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
HBB hemoglobin, beta