Disease Index

Lichstenstein syndrome is characterised by frequent infections associated with osteoporosis, a tendency for fractures and osseous anomalies. It has been described in two monozygotic twin brothers. Transmission is autosomal recessive.

genetic disorder inherited in an autosomal dominant manner that is characterized by early, and frequently severe, high blood pressure

human disease

human disease

medical condition

medical condition

Limb body wall complex (LBWC) is characterized by severe multiple congenital anomalies in the fetus with exencephaly/encephalocele, thoraco- and/or abdominoschisis (anterior body wall defects) and limb defects, with or without facial clefts

congenital genetic disorder which causes oligodactyly and micrognathia

muscular dystrophy characterized by weakening of the muscles of the hip and shoulders which comprise the limb girdle muscles

human disease

loss or disturbance of limbal stem cell function in the corneal limbus

inflammation involving the limbic system in the brain

human disease

human disease

human disease

the least progressive form of systemic scleroderma with skin thickening restricted to the face, neck and areas distal to the elbows and/or knees, sparing the trunk

Limited systemic sclerosis (lSSc) (or SSc sine scleroderma) is a subset of systemic sclerosis (SSc; see this term) characterized by organ involvement in the absence of fibrosis of the skin

medical condition

medical condition

human disease

Human disease

Linear lichen planus (LLP), also referred to as Blaschkoid LP, is a rare type of lichen planus characterized by a linear distribution of lichenoid lesions along the lines of Blaschko, which are embryonic pathways of skin development

human disease

Human disease

human disease

disorder where there is enlargement of both legs due to deposits of fat under the skin

abnormal levels of cholesterol & lipids