Additional Disease Briefs

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Rare Disease Database Reports Additional Rare Disease Briefs
hemochromatosis type 5

Also known as: FTH1 hereditary hemochromatosis, FTH1-associated iron overload, FTH1-related iron overload, HFE5, hemochromatosis, type 5, hereditary hemochromatosis caused by mutation in FTH1, iron overload, autosomal dominant

hemoglobin H disease

Also known as: Alpha-thalassemia intermedia, Alpha-thalassemia, Haemoglobin H type, Alpha-thalassemia, Hemoglobin H type, HBA1;HBA2 digenic triallelic hemoglobin H disease, HBH, HEMOGLOBIN H disease, Haemoglobin H disease, Deletional, Haemoglobin H disease, Nondeletional, HbH, HbH disease, Hemoglobin H disease, Deletional, Hemoglobin H disease, Nondeletional, alpha thalassemia, haemoglobin H type, alpha thalassemia, hemoglobin H type, alpha-thalassemia intermedia, haemoglobin H disease, deletional, haemoglobin H disease, deletional and nondeletional, hemoglobin H disease, hemoglobin H disease caused by triallelic variation in HBA1;HBA2, hemoglobin H disease related to triallelic variation in HBA1 and HBA2, hemoglobin H disease, deletional, hemoglobin H disease, deletional and nondeletional

hemoglobin M disease

Also known as: M hemoglobinopathy, autosomal dominant methemoglobinemia, blue baby syndrome, hereditary methemoglobinemia due to haemoglobin mutation, hereditary methemoglobinemia due to hemoglobin mutation, methemoglobinemia, beta type, methemoglobinemia, beta-globin type

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