Disease Directory

ALECT2 amyloidosis is a rare form of amyloidosis where a protein called leukocyte chemotactic factor-2 (LECT2) builds up in body tissues. This protein...

ALG1-CDG is a severe congenital disorder that affects many systems in the body. It disrupts a process called N-linked glycosylation, which is importan...

ALG10-congenital disorder of glycosylation is a rare genetic condition that falls under the group of congenital disorders of glycosylation. This condi...

ALG11-congenital disorder of glycosylation is a rare genetic condition that affects the body’s ability to properly add sugars to proteins, a process k...

ALG12-congenital disorder of glycosylation is a rare condition that affects how proteins are modified in the body. People with this condition may have...

ALG14-congenital disorder of glycosylation, also known as ALG14-CDG, is a rare condition caused by a deficiency in the ALG14 enzyme. This enzyme plays...

ALG2-congenital disorder of glycosylation is a rare genetic condition that affects the process of glycosylation, which is important for normal cell fu...

ALG3-congenital disorder of glycosylation is a rare metabolic condition that affects how sugars attach to proteins in the body. This condition is one...

ALG6-congenital disorder of glycosylation 1C is a type of congenital disorder that affects the process of glycosylation, which is how sugars attach to...

ALG8-congenital disorder of glycosylation is a rare inherited condition that affects how proteins in the body are modified by a process called glycosy...

ALG9-associated autosomal dominant polycystic kidney disease is characterized by mutations in the ALG9 gene, leading to a form of autosomal dominant p...

ALG9-congenital disorder of glycosylation is a condition that affects the way sugars attach to proteins in the body. This disorder belongs to a group...

ALK-negative anaplastic large cell lymphoma (ALK- ALCL) is a type of ALCL, a rare and aggressive peripheral T-cell non-Hodgkin lymphoma that affects l...

ALK-positive anaplastic large cell lymphoma is a rare and aggressive form of non-Hodgkin lymphoma that affects lymph nodes as well as other parts of t...

ALK-positive large B-cell lymphoma is a very rare type of diffuse large B-cell lymphoma. It mainly affects middle-aged people, especially men who have...

ALPI-related inflammatory bowel disease is an inflammatory bowel condition caused by a mutation in the ALPI gene. This condition affects the intestine...

ALPL-related autosomal dominant hypophosphatasia is a type of hypophosphatasia. In this condition, a change in the ALPL gene causes problems with the...

ALPL-related autosomal recessive hypophosphatasia is a form of hypophosphatasia caused by a loss-of-function in the ALPL gene that follows an autosoma...

ALS2-related motor neuron disease is a type of motor neuron disease that occurs because of a mutation in the ALS2 gene. Motor neuron diseases affect t...

Information about overview is currently limited for this condition.