<owl:Class xmlns="https://folio.openlegalstandard.org/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:v1="http://www.loc.gov/mads/rdf/v1#" xmlns:owl="http://www.w3.org/2002/07/owl#" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:xsd="http://www.w3.org/2001/XMLSchema#" xmlns:folio="https://folio.openlegalstandard.org/" xmlns:rdfs="http://www.w3.org/2000/01/rdf-schema#" xmlns:skos="http://www.w3.org/2004/02/skos/core#" rdf:about="https://folio.openlegalstandard.org/R7PdNH9CyPCZwagGc0NzW76">
  <rdfs:subClassOf rdf:resource="https://folio.openlegalstandard.org/Ri4LGaOgWzMWy2yX79DQi0"/>
  <rdfs:label>Hemoglobin Deficiency</rdfs:label>
  <skos:prefLabel>Thalassemia</skos:prefLabel>
  <skos:definition>Thalassemia is a genetic blood disorder characterized by the reduced production of hemoglobin, leading to anemia and other related health issues. It is caused by mutations in the genes responsible for hemoglobin production, resulting in abnormal hemoglobin and red blood cells.</skos:definition>
</owl:Class>
