5-hydroxytryptamine receptor 1A (HTR1A)
Rubella Antibody, IgG
Hepatitis E Virus (HEV) Antibody, IgG
T-Cell Receptor Gene Rearrangement, Flow Cytometry, Bone Marrow
Normetanephrine, Plasma
Calcium Channel Voltage-dependent L Type alpha 1S Subunit (CACNA1S) Gene Mutation Analysis
Idiopathic Pulmonary Fibrosis Diagnostic Test (Envisia™)
Oxcarbazepine, Serum
Autoinflammatory Primary Immunodeficiency (PID) Gene Panel
Alveolar Soft Part Sarcoma (ASPS)/Renal Cell Carcinoma (RCC), Xp11.23 (TFE3), FISH, Tissue
LDS
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Rare Constitutional and hereditary Diseases, Whole Exome Sequence Analysis, NGS
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Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
LOINC
ICD10
Additional ICD10
References
All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
LOINC
ICD10
Additional ICD10
References
Rare Constitutional and hereditary Diseases, Whole Exome Sequence Analysis, NGS
Medical Test
Specimen Collection
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Rare Constitutional and hereditary Diseases, Whole Exome Sequence Analysis, NGS
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