Disease Index

human disease

human disease

an inborn error of cholesterol synthesis, caused by a mutation in the enzyme 7-Dehydrocholesterol reductase

Human disease

osteochondrodysplasia characterized by short limbs and a short trunk with a barrel-shaped chest and has material basis in homozygous or compound heterozygous mutation in the DYM gene on chromosome 18q

medical condition

injury caused by a bite from a snake

form of arteriopathy

medical condition

Human disease

human disease

medical condition

neoplasm that arises from soft tissue

human disease

skin disease

medical condition

human disease

Human disease

human disease

human disease

Human disease

human disease

hyperostosis that has material basis in a mutation in the SOST gene which results in overgrowth of endosteal bone producing dense and wide bones throughout the body especially located in skull

autosomal recessive disease that occurs rarely and is characterized by excessive physical growth during the first 2 to 3 years of life

medical condition