Disease Index

infectious disease characterized by severe form of infection producing pneumonia

rare genetic skin pigmentation disorder characterized by multiple cafe-au-lait macules

mitochondrial metabolism disease characterized by progressive loss of mental and movement abilities. Symptoms usually begin between ages of three months and two years and include loss of appetite, vomiting, irritability and seizure activity

human disease

human disease

human disease

human disease

disease

malignant smooth muscle cancer that can arise almost anywhere in the body, but is most common in the uterus, abdomen, or pelvis

Lelis syndrome is characterised by the association of ectodermal dysplasia (hypotrichosis and hypohidrosis) with acanthosis nigricans

Human disease: infectious thrombophlebitis of the internal jugular vein

rare but severe childhood-onset epilepsy

Human disease

human disease

human disease

human disease

human disease

Lenz-Majewski hyperostotic dwarfism is an extremely rare syndrome associating dwarfism, characteristic facial appearance, cutis laxa and progressive bone sclerosis

rare autosomal dominant,[3] multisystem disease caused by a mutation in the protein tyrosine phosphatase, non-receptor type 11 gene (PTPN11)

chronic infection caused by bacteria Mycobacterium leprae

human disease

human and animal infectious disease

medical condition

human disease

rare genetic syndrome

Lethal acantholytic epidermolysis bullosa is a suprabasal subtype of epidermolysis bullosa simplex (EBS, see this term) characterized by generalized oozing erosions, usually in the absence of blisters

human disease

human disease

human disease