TTC37 gene
The TTC37 gene, also known as Trichohepatoenteric syndrome (TCS), is associated with a rare genetic syndrome characterized by hair, liver, and intestinal…
PHGDH gene
The PHGDH gene, also known as phosphoglycerate dehydrogenase, is a genetic condition that affects the production of phosphoglycerate in the body. This…
PKLR gene
The PKLR gene, also known as the pyruvate kinase liver and red blood cell (PKLR) gene, is a genetic molecule that plays…
NAGLU gene
The NAGLU gene, also known as N-acetylglucosaminidase alpha, is responsible for encoding an enzyme that plays a crucial role in the breakdown…
EDAR gene
The EDAR gene is a gene that has been extensively studied and researched in the field of genetics. It is one of…
MMAA gene
The MMAA gene, also known as methylmalonic aciduria (MMA) gene, is related to the mutase methylmalonic acidemia. It is listed in the…
Congenital leptin deficiency
Congenital leptin deficiency is a rare genetic condition associated with severe early-onset obesity. This condition is caused by mutations in the genes…
MMUT gene
The MMUT gene, also known as the Methylmalonyl-CoA Mutase gene, is a gene that encodes the enzyme methylmalonyl-CoA mutase. This gene is…
DCXR gene
The DCXR gene, also known as the dicarbonyl/xylose reductase gene, is listed in various scientific databases as an essential gene involved in…