Familial Hypercholesterolemia and Related Diseases Multi-Gene Panel, NGS
Filaria Antibody, IgG4
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
LDS
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Angelman syndrome
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Additional ICD10
SNOMED
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ICD10
Additional ICD10
SNOMED
Angelman syndrome
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