The UROS gene, also known as uroporphyrinogen III synthase, is responsible for producing an enzyme involved in the production of heme. Heme…

The DVL3 gene is a genetic effect related gene that has been extensively studied. According to PubMed, this variant has been linked…

Genetic ancestry testing, sometimes referred to as direct-to-consumer genetic testing, is a type of testing that provides information about an individual’s genetic…

Microcephalic osteodysplastic primordial dwarfism type II (MOPD II) is a rare genetic condition characterized by severe growth retardation and developmental abnormalities. It…

The CAPN3 gene, also known as calpain-3, is a genetic enzyme that plays a crucial role in muscle function. It is primarily…

Alexander disease is a rare genetic disorder of the central nervous system. It is a glial disease named after Stewart Alexander, who…

Mucolipidosis III alphabeta, also known as MLIII alphabeta, is a rare genetic disorder that causes progressive damage to various tissues and organs…

Glucose phosphate isomerase deficiency, also known as GPI deficiency, is a rare genetic disorder that affects the glucose-6-phosphate isomerase enzyme. This enzyme…

Giant axonal neuropathy (GAN) is a rare genetic disorder that affects the central nervous system. It is characterized by the progressive destruction…