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...

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...

Lichen amyloidosis is a rare chronic form of cutaneous amyloidosis, a skin condition characterized by the deposition of amyloid in the dermis, which r...

Lichen myxedematosus is a skin disorder marked by changes in the skin's texture and the appearance of papules, often described as mucin deposits. Alth...

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...

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

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...

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

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

Ligament disorder is a condition that affects the connective tissues responsible for stabilizing joints. It involves abnormalities of the ligament, wh...

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

Light and heavy chain deposition disease, also known as LHCDD, is a condition characterized by the abnormal deposition of protein components in tissue...

Light chain deposition disease is a rare condition in which small protein fragments called light chains accumulate in the kidneys and can also affect...