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56,145 results found
You searched for “Y” in All. RX Search found 56,145 result(s) and checks doctor-selected, exact-title, synonym, and related matches.
Congenital brachyesophagus-intrathoracic stomach-vertebral anomalies syndrome is an ultra-rare birth defect syndrome. It is also called a rare syndromic esophageal malformation. In this condition, the food pipe,...
Liver disease-retinitis pigmentosa-polyneuropathy-epilepsy syndrome is a very rare inherited metabolic disease. It is also called alpha-methylacyl-CoA racemase deficiency, AMACR deficiency, or congenital bile acid synthesis defect...
Intrahepatic cholestasis with defective conversion of trihydroxycoprostanic acid to cholic acid is a very rare inherited bile acid synthesis disorder. It is now usually called congenital...
Alpha-methyl-acyl-CoA racemase deficiency, often shortened to AMACR deficiency, is a very rare inherited metabolic disease. It happens when the body cannot make enough working alpha-methyl-acyl-CoA racemase...
2-methylacyl-CoA racemase deficiency is a very rare inherited metabolic disease. It happens when the body does not make enough working AMACR enzyme. This enzyme helps break...
Congenital bile acid synthesis defect 4, also called CBAS4 or AMACR deficiency, is a very rare inherited disorder caused by harmful changes in the AMACR gene....
CYP7B1 oxysterol 7-alpha-hydroxylase deficiency is a very rare inherited disease. It happens when both copies of the CYP7B1 gene do not work properly. This gene normally...
Congenital bile acid synthesis defect caused by mutation in CYP7B1 is a very rare inherited liver disease. Its best known medical name is congenital bile acid...
Congenital bile acid synthesis defect 3, also called CBAS3 or oxysterol 7 alpha-hydroxylase deficiency, is a very rare inherited liver disease caused by harmful changes in...
Congenital bile acid synthesis defect caused by mutation in AKR1D1 is also called congenital bile acid synthesis defect type 2, CBAS2, or delta-4-3-oxosteroid 5-beta-reductase deficiency. It...
AKR1D1 congenital bile acid synthesis defect is a very rare inherited liver and metabolism disease. Its usual formal name is congenital bile acid synthesis defect type...
Congenital bile acid synthesis defect 2 is a very rare inherited liver disease. It happens when the body cannot make normal bile acids in the right...
