Hereditary Nonpolyposis Colorectal Cancer (Lynch syndrome)
c-KIT Mutation Analysis, Melanoma
Mucopolysaccharidosis type I
Hemoglobin S, Screen, Blood
Zollinger-Ellison syndrome (gastrinoma)
Triiodothyronine (T3), Free
PPP2R2B (Protein Phosphatase 2 Regulatory Subunit Beta) Gene Mutation Analysis
Alpha-actinin-2 (ACTN2) Gene Analysis
Amyloid Beta Protein (β1-40 and Aβ1-42)
UDP Glucuronosyltransferase 1A1 (UGT1A1) Genotyping
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Acute intermittent porphyria
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Acute intermittent porphyria
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SNOMED
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