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Lactose intolerance is when people lack lactase, which breaks lactose into a form that can be absorbed by the blood.

Lupus causes the immune system to mistakenly attack the body. It’s unpredictabe: It can affect many parts of the body at the same time.

Lysosomal acid lipase deficiency is a subset of lysosomal acid lipase deficiency (LALD).

Labial hypoplasia is a harmless condition in which one or both sides of the labia don't form normally during puberty.

Li-Fraumeni syndrome is a hereditary condition that is often associated with a pathogenic variant in the TP53 gene.

Mucopolysarcharidosis type IVB (MPS IVB), also known as Morquio syndrome type B, is a rare, inherited disorder in which genetic variations disrupt the normal activity of lysosomes in human cells.

Mucopolysarcharidosis type VI (MPS VI), also known as Maroteaux-Lamay syndrome, is a rare, inherited disorder in which genetic variations disrupt the normal activity of lysosomes in human cells.

Metachromatic leukodystrophy is a rare genetic condition in which an abnormal accumulation of fat molecules (sulfatides) affects cells in the nervous system.

Multiple sulfatase deficiency is a complex, inherited disorder caused by a genetic mutation.