Leukoencephalopathy with vanishing white matter is a disorder affecting the brain's white matter and is classified among the leukodystrophies. Recogni...

Leukoencephalopathy with vanishing white matter 1 is a disorder primarily affecting the brain’s white matter, leading to progressive neurological impa...

Leukoencephalopathy with vanishing white matter 5 is a neurologic disorder that affects the brain’s white matter, leading to progressive deterioration...

Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome is a very rare ectodermal dysplasia syndrome. It is characteriz...

Leukopenia is a laboratory finding that indicates a decreased number of white blood cells in the peripheral blood, which are essential for fighting in...

Lewis-Sumner syndrome is a rare nerve disorder that affects adults. It is an acquired demyelinating polyneuropathy, which means that the protective co...

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...

L-ferritin deficiency is a rare genetic condition known by several names including L-ferritin deficiency, dominant and recessive L-ferritin deficiency...