1p36.3 Microdeletion Syndrome, FISH
Apolipoprotein B, Serum
Cephalosporin IgE
PML-RARA (Promyelocytic Leukemia/Retinoic Acid Receptor Alpha) Translocation, t(15;17) Analysis
Psychosis, unspecified
Factor IX Gene Gene Mutation Analysis
Specific Gravity, Body Fluid
CaM Kinase II (CaMKII, Calcium-dependent Calmodulin Protein Kinase II) Activation
Meprobamate, Urine
4q25 Atrial Fibrillation Risk Genotype Test
LDS
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Myeloid Differentiation Primary Response 88 (MYD88) Gene Mutation Analysis
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
Myeloid Differentiation Primary Response 88 (MYD88) Gene Mutation Analysis
Medical Test
ICD10
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Myeloid Differentiation Primary Response 88 (MYD88) Gene Mutation Analysis
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