Disease Directory

Lewy body dementia is a progressive form of dementia. It is marked by specific protein deposits called Lewy bodies found in the midbrain and cerebral...

Leydig cell hypoplasia is a condition that affects male sexual development. It occurs when the Leydig cells in the testes are underdeveloped. These ce...

Leydig cell hypoplasia due to complete LH resistance is a rare condition that affects the development of sex characteristics. It is often referred to...

Information about overview is currently limited for this condition.

Leydig cell hypoplasia, type 1 is a condition caused by a mutation in the LHCGR gene. The mutation affects the function of Leydig cells, which are imp...

Lhermitte-Duclos disease (LDD) is a very rare condition where the cerebellum, a part of the brain that helps control movement and balance, develops ab...

Li-Fraumeni syndrome is an inherited condition that increases the risk of several types of cancer. This condition follows an autosomal dominant patter...

Li-Ghorbani-Weisz-Hubshman syndrome, also known as Li-Ghorgani-Weisz-Hubshman syndrome or LIGOWS, is a rare condition with very limited publicly avail...

Li-fraumeni-like syndrome is a rare disease. Detailed information about this condition is currently limited in medical literature.

Liang-Wang syndrome, also known as LIWAS, is a rare medical condition that is recorded in major rare disease databases such as OMIM (OMIM:618729) and...

Liberfarb syndrome is a progressive condition that affects several body systems, including the eyes, ears, bones, and brain. It is a connective tissue...

Lichtenstein syndrome is a rare genetic condition that has been reported in two monozygotic twin brothers. People with this syndrome experience freque...

Lichtenstein-Knorr syndrome is a rare genetic condition that affects the brain and other parts of the body. It is characterized by early-onset problem...

Liddle syndrome is a rare genetic condition that leads to high blood pressure. It is characterized by low renin levels in the blood along with decreas...

Liddle syndrome 1 is a rare condition that happens because of a mutation in the SCNN1B gene. This change in the gene affects how the body handles sodi...

Liddle syndrome 2 is a rare genetic condition caused by a mutation in the SCNN1G gene. This mutation affects the protein that controls sodium channels...

Liddle syndrome 3, also known as LIDLS3, is a rare condition with limited detailed descriptions available in the literature. The condition is recogniz...

Lisch epithelial corneal dystrophy (LECD) is a very rare disorder that affects the surface of the cornea, the clear front part of the eye. It is marke...

Listeria meningitis is an infection where the membranes covering the brain and spinal cord become inflamed due to the bacteria Listeria monocytogenes....

Loeffler endocarditis is a rare restrictive cardiomyopathy where high levels of eosinophils (a type of white blood cell) cause damage to the heart. Th...