Disease Index

condition in which the blood’s ability to coagulate (form clots) is impaired

rare genetic disorder with short strature and predisposition to cancer

osteochondrodysplasia that results in inward turning of lower leg, located in tibia, which fails to develop normally

Human disease

Blue Diaper syndrome is a hereditary metabolic disorder characterised by hypercalcaemia with nephrocalcinosis and indicanuria

rare vascular malformation disorder with cutaneous and visceral lesions frequently associated with serious, potentially fatal bleeding and anemia

human disease

Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency is a very rare genetic skin disease characterized by severe skin laxity affecting the trunk and limbs

rare genetic syndrome caused by a mutation in the ASXL1 gene

hemorrhagic fever and zoonotic infectious disease originating in Bolivia after infection by Machupo virus

connective tissue cancer that is located in bone and is characterized by uncontrolled cellular proliferation that destroys normal bone tissue

bone disease that results in abnormal growth and development located in bone or located in cartilage

bone cancer and lymphoma by site that results in lymphoma starting in the bone

a sarcoma that arises from the bone, for example osteosarcoma and chondrosarcoma

disease

disease

Human disease

low grade epithelial tumor arising from the ovary. It is characterized by an atypical proliferation of epithelial cells. There is no evidence of stromal invasion

genetic condition in humans

hereditary disease

Human disease

human and animal disease

Human disease

human disease

Human disease