Glycogen Storage Disease Type 0: Symptoms and Lifestyle Management disease
Glycogen Storage Disease Type 0, also known as glycogen synthase deficiency, is related to hypoglycemia and glycogen storage disease. An important gene associated with Glycogen Storage Disease Type 0 is GYS2 (Glycogen Synthase 2), and among its related pathways/superpathways are Metabolism and Disease. The drug Pharmaceutical Solutions has ...
Birk-Barel Syndrome: Autoimmune Disorder and Management disease
Birk-Barel Syndrome, also known as birk-barel mental retardation dysmorphism syndrome, is related to kcnk9 imprinting syndrome and hypotonia. An important gene associated with Birk-Barel Syndrome is KCNK9 (Potassium Two Pore Domain Channel Subfamily K Member 9), and among its related pathways/superpathways are Activation of cAMP-Dependent ...
Manage Orthostatic Hypotension: Lifestyle Tips disease
Pure Autonomic Failure, also known as orthostatic hypotension, is related to multiple system atrophy 1 and dementia, lewy body. An important gene associated with Pure Autonomic Failure is DBH (Dopamine Beta-Hydroxylase), and among its related pathways/superpathways are Neuroscience and superpathway of tryptophan utilization. The drugs ...
LGMD: CAPN3 Gene and Symptom Management disease
Limb-Girdle Muscular Dystrophy, also known as lgmd, is related to muscular dystrophy, limb-girdle, autosomal recessive 1 and muscular dystrophy, limb-girdle, autosomal dominant 3. An important gene associated with Limb-Girdle Muscular Dystrophy is CAPN3 (Calpain 3), and among its related pathways/superpathways are Cardiac conduction and ...
Glutaric Aciduria Type 1: Lifestyle and Management disease
Glutaric Acidemia I, also known as glutaryl-coa dehydrogenase deficiency, is related to multiple acyl-coa dehydrogenase deficiency and 2-hydroxyglutaric aciduria, and has symptoms including muscle rigidity and opisthotonus. An important gene associated with Glutaric Acidemia I is GCDH (Glutaryl-CoA Dehydrogenase), and among its related ...