Complement Component C1q
Heparin Antifactor Xa Assay
Neurotrophic Receptor Tyrosine Kinase 1 (NTRK1) Gene Mutation Analysis (Translocation)
Hemoglobin A1c
PTPN22 Genotype, 1858C->T for Rheumatoid arthritis (RA)
Respiratory distress syndrome of the newborn
Cowden Syndrome
Follicular Lymphoma, bcl-2/JH t(14;18), FISH
Hereditary diffuse gastric cancer
Estradiol, Serum
LDS
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Peritonitis
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Medical Tests
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ICD10
Additional ICD10
SNOMED
Peritonitis
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Additional ICD10
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