WIPF1 Gene Mutation Analysis
Kallmann Syndrome, Xp22.3 Deletion, FISH
ACTH Stimulation Test (Cosyntropin)
Biopsy, Pericardial
Carnitine, Total, Serum/Plasma
Amyloid Beta Protein Ratio 1-42/1-40, Spinal Fluid
Neurofibromatosis Type 1 (NF1) Gene Mutation Analysis
Citrate Excretion for Kidney Stones, Random, Urine
Gene Expression Profile for Cutaneous Melanoma, DermTech (DecisionDx®-SCC), Pigmented Lesion Assay (PLA), myPath® Melanoma
Triglycerides, Body Fluid

Myocarditis
Disease