Salmonella infections and gastroenteritis
Usher Syndrome, Types 1F and 3 (PCDH15 and CLRN1), 2 Variants
Hyperprolactinemia
Familial Dysautonomia Genetic Mutation Analysis
Phospholipase A2 Receptor (PLA2R) Antibody, IgG
Narcolepsy (HLA-DQB1*06:02P) Genotyping
Thiothixene (Navane), Urine
Benign neoplasm, spinal cord
Mini Respiratory Pathogen Panel (Influenza A and B and SARS-CoV-2), Molecular
Dysmenorrhea
LDS
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Neurotrophic Receptor Tyrosine Kinase 2 (NTRK2) Gene Mutation Analysis (Translocation)
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ICD10
Additional ICD10
All
Diseases
CPT
LOINC
ICD10
Additional ICD10
Neurotrophic Receptor Tyrosine Kinase 2 (NTRK2) Gene Mutation Analysis (Translocation)
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Diseases (25)
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