Carbohydrate Deficient Transferrin for Congenital Disorders of Glycosylation, Serum
Immunoglobulin E (IgE)
Chromosome Analysis, Interphase, FISH
Atopic Dermatitis
Benign neoplasm of liver and/or biliary ducts
Human Immunodeficiency Virus 2 (HIV-2) DNA/RNA Qualitative or Quantitative
Interleukin 6 (IL-6), Serum
Lyme Disease (Borrelia burgdorferi) Antibody, IgG and IgM
Estrogen/Progesterone Receptor, IHC, Semi-Quantitative
Atypical Pneumonia DNA Panel, Bronchial Wash/Lavage
LDS
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Primary Hyperoxaluria Gene Mutation Panel
All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
ICD10
Additional ICD10
References
All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
ICD10
Additional ICD10
References
Primary Hyperoxaluria Gene Mutation Panel
Medical Test
ICD10
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Primary Hyperoxaluria Gene Mutation Panel
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