Treponema pallidum Antibody, IgG by IFA (FTA-ABS), Serum
Neuron Specific Enolase (NSE), CSF
Lymphocytic Choriomeningitis (LCM) Virus Antibody, IgM
TNNI3 (Troponin I) Gene Mutation Analysis
PDGFRA (platelet-derived growth factor receptor, alpha polypeptide) Gene Mutation Analysis
Pneumocystis jirovecii, DFA
Mucopolysaccharides (MPS), Acid, Quantitative, Urine
Anaplasma phagocytophilum Molecular Detection, PCR
UBE3A Gene Mutation Analysis, Angelman Syndrome, Tissue
Beta-2 Microglobulin, Spinal Fluid

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/Medical Tests
/von Willebrand Disease 2N (Subtype Normandy), Genotyping

All
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

von Willebrand Disease 2N (Subtype Normandy), Genotyping
Medical Test

Access to von Willebrand Disease 2N (Subtype Normandy), Genotyping is restricted.