Version: 8.0.0
Date: Tue Jan 28 2025
2 results for acadm
Disease

medium chain acyl-CoA dehydrogenase deficiency

Disease
Source: DOID:0080153
Definition: A lipid metabolism disorder that is characterized by a deficiency of the enzyme medium chain acyl-CoA dehydrogenase that results in the inability to convert medium chain fatty acids to energy, particularly during fasting.
Genes: acadm.L (Xla)...Acadm (Mmu)...acadm (Xtr)...ACADM (Hsa)...acadm (Dre)
Alleles: Acadm (Mmu)

metabolic dysfunction-associated steatotic liver disease

Disease
Source: DOID:0080208
Definition: A steatotic liver disease characterized by at least one of five specified cardiometabolic risk factors and no other discernible cause with normal to no alcohol use. The five cardiometabolic risk factors are: (1) higher than normal body mass index or waist circumference; (2) higher than normal serum glucose or glycated hemoglobin level, or type 2 diabetes; (3) higher than normal blood pressure or hypertensive treatment; (4) higher than normal plasma triglycerides or lipid lowering treatment; and (5) lower than normal plasma high-density lipoprotein cholesterol.
Genes: Acadm (Rno)...Acadm (Mmu)...ACADM (Hsa)...acadm (Xtr)...acadm (Dre)