HEMOGLOBIN H DISEASE; HBH |
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HEMOGLOBIN, HIGH ALTITUDE ADAPTATION; HALAH |
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HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO GLUCOSE PHOSPHATE ISOMERASE DEFICIENCY |
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HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 1; AHUS1 |
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HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 3; AHUS3 |
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HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 6; AHUS6 |
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HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1; FHL1 |
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HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2; FHL2 |
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HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 3; FHL3 |
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HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 4; FHL4 |
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HEMOPHILIA B; HEMB |
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HEMORRHAGE, INTRACEREBRAL, SUSCEPTIBILITY TO; ICH |
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HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 2; HKLLS2 |
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HENNEKAM SYNDROME |
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HEPARIN COFACTOR II DEFICIENCY |
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HEPATIC ADENOMAS, FAMILIAL |
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HEPATIC VENOOCCLUSIVE DISEASE WITH IMMUNODEFICIENCY; VODI |
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HEPATITIS B VIRUS, SUSCEPTIBILITY TO |
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HEPATOCELLULAR CARCINOMA |
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HEPATOERYTHROPOIETIC PORPHYRIA |
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