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- NCIT_C95504 IAO_0000115 "A form of alpha thalassemia that results from reduced protein production from three of the four alpha-globin genes. Clinically it is characterized by chronic hemolytic anemia." @default.
- NCIT_C95504 NCIT_NHC0 "C95504" @default.
- NCIT_C95504 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C95504 NCIT_P108 "Hemoglobin H Disease" @default.
- NCIT_C95504 NCIT_P207 "C3161174" @default.
- NCIT_C95504 NCIT_P322 "NICHD" @default.
- NCIT_C95504 NCIT_P325 "A form of alpha thalassemia that results from reduced protein production from three of the four alpha-globin genes. Clinically it is characterized by chronic hemolytic anemia." @default.
- NCIT_C95504 NCIT_R100 NCIT_C12219 @default.
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- NCIT_C95504 NCIT_R115 NCIT_C7057 @default.
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- NCIT_C95504 NCIT_R176 NCIT_C75432 @default.
- NCIT_C95504 normalizedInformationContent "100" @default.
- NCIT_C95504 referenceCount "1" @default.
- NCIT_C95504 hasExactSynonym "Hemoglobin H Disease" @default.
- NCIT_C95504 inSubset NCIT_C132009 @default.
- NCIT_C95504 inSubset NCIT_C90259 @default.
- NCIT_C95504 type Class @default.
- NCIT_C95504 isDefinedBy ncit.owl @default.
- NCIT_C95504 label "Hemoglobin H Disease" @default.
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- NCIT_C95504 subClassOf NCIT_C95504 @default.