LADD syndrome is a rare congenital disorder where multiple body systems are affected. People with this condition often have abnormalities in the tear...

LADD syndrome 1 is a rare genetic condition caused by a variation in the FGFR2 gene. This condition affects multiple parts of the body and is sometime...

Lafora disease (LD) is a rare, inherited condition characterized by severe progressive myoclonic epilepsy. It is caused by variants in the NHLRC1 and...

LAMA2-related muscular dystrophy is a form of muscular dystrophy that is caused by a mutation in the LAMA2 gene. This condition affects muscle strengt...

LAMA5-related multisystemic syndrome is a rare genetic disorder that affects multiple parts of the body. It is characterized by symptoms that begin in...

Lambert-Eaton myasthenic syndrome is an autoimmune disorder that affects neuromuscular transmission, resulting in fluctuating muscle weakness and auto...

Lambert syndrome is a very rare condition that was first described in four siblings from one French family. The syndrome is characterized by a set of...

Information about overview is currently limited for this condition.

Lamellar ichthyosis is a keratinization disorder that primarily affects the skin, leading to the development of large, plate-like scales covering much...

Laminopathy is a rare genetic condition that arises from mutations affecting proteins of the nuclear lamina. It is caused by alterations in the genes...

Landau-Kleffner syndrome is a rare form of epileptic encephalopathy. It is marked by abnormal spike-wave brain activity during sleep. This condition c...

Lane Hamilton syndrome is a rare condition where idiopathic pulmonary hemosiderosis and celiac disease occur together. It is most commonly seen in chi...

Langerhans cell histiocytosis is a systemic condition characterized by the abnormal proliferation and accumulation of Langerhans cells in various tiss...

Langerhans cell histiocytosis specific to adulthood is a condition that primarily manifests in adults and includes recognized subtypes, such as adult...

Langerhans cell histiocytosis specific to childhood is a condition characterized by an abnormal accumulation of Langerhans cells, which can lead to va...

Langerhans cell sarcoma is a rare type of cancer that involves a fast-growing proliferation of Langerhans cells, a type of immune cell found in the sk...

Langer mesomelic dysplasia (LMD) is a rare condition characterized by severe disproportionate short stature. People with this condition experience sho...

Large-cell immunoblastic lymphoma is a type of malignant lymphoma that affects the lymphatic system and is characterized by the presence of immunoblas...