Disease Index

human disease

human disease

human disease

Human disease

human disease

calcinosis that is the calcification or a bony hardening of ligaments in areas where they attach to the spine

type of lymphoma (cancer)

diffuse large B-cell lymphoma arising from the central nervous system

medical condition

human disease

human disease

highly aggressive brain tumor, mostly found in children

a progressive demyelinating disorder of the central nervous system

medical condition

human disease

inflammatory lung disease

Human disease

variant of systemic scleroderma characterized by sclerosis of the skin, Raynaud phenomenon, and organ involvement, including pulmonary fibrosis, renal disease, and gastrointestinal tract involvement

T cell deficiency disease that is the result of a large deletion of chromosome 22, which includes the DGS gene needed for development of the thymus and related glands with subsequent lack of T-cell production

human disease

congenital structural abnormalities of the digestive system

human disease

medical condition

purine-pyrimidine metabolic disorder that is an autosomal recessive metabolic disorder in which there is absent or significantly decreased activity of dihydropyrimidine dehydrogenase, an enzyme involved in the metabolism of uracil and thymine

disease characterized by an enlarged heart

dilated cardiomyopathy that has material basis in mutation in the LMNA gene on chromosome 1q21