Summary

Erythrocyte Lactate Transporter Defect, also known as metabolic myopathy due to lactate transporter defect,is related to monocarboxylate transporter 1 deficiency and hyperinsulinemic hypoglycemia, familial, 7,and has symptoms including elevated serum creatine phosphokinase, exercise-induced muscle cramps and exercise-induced muscle stiffness. An important gene associated with Erythrocyte Lactate Transporter Defect is SLC16A1 (Solute Carrier Family 16 Member 1)

All SNPs

Disease Hierarchy

Disease Interacts with Genes

Disease Interacts with Substances

Processes Associated With Trait

Pathways Associated With Trait

Symptoms Associated With Trait