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- Be26e076272de5862e3e6073a55239d1e hasDbXref "Orphanet:231230" @default.
- Be26e076272de5862e3e6073a55239d1e type Axiom @default.
- Be26e076272de5862e3e6073a55239d1e annotatedProperty IAO_0000115 @default.
- Be26e076272de5862e3e6073a55239d1e annotatedSource MONDO_0016488 @default.
- Be26e076272de5862e3e6073a55239d1e annotatedTarget "OBSOLETE. Beta-thalassemias associated with hemoglobin (Hb) anomalies result in a variable clinical spectrum, ranging from asymptomatic to severe, depending on the severity of the thalassemia mutation and on the type of the Hb anomaly [hereditary persistence of fetal Hb, delta-beta-thalassemia, Hb C - beta-thalassemia, Hb E - beta-thalassemia and Hb S - beta-thalassemia ]." @default.