Disease Index

tumor of the central nervous system that originates from the vascular system

human disease

human disease

medical procedure to replace bone marrow stem cells

disorder which primarily affects the blood

human disease

primary headache disorder

human disease

human disease

human disease

medical condition

a rare disorder affecting development of one side of the brain

congenital deficiency of one or more limbs

migraine with aura

hemochromatosis that has material basis in homozygous or compound heterozygous mutation in the HFE gene on chromosome 6p22

hemochromatosis characterized by autosomal recessive inheritance of early onset of severe iron loading with symptoms including; hypogonadotropic hypogonadism, cardiomyopathy, arthropathy, and liver fibrosis or cirrhosis

hemochromatosis that has material basis in homozygous or compound heterozygous mutation in the TFR2 gene on chromosome 7q22

hemochromatosis that has material basis in heterozygous mutation in the SLC40A1 gene on chromosome 2q32

hemochromatosis that has material basis in heterozygous mutation in the FTH1 gene on chromosome 11q12

Human disease

Hemoglobin C - beta-thalassemia (HbC - BT) is a form of beta-thalassemia (see this term) resulting in moderate hemolytic anemia

Human disease

variant form of human hemoglobin

alpha thalassemia that has material basis in contiguous gene deletion of the hemoglobin alpha-1 (HBA1) and alpha-2 (HBA2) genes on one chromosome 16, and a defect, deletional or nondeletional, in either HBA1 or HBA2 on the other

human disease

human disease