Aminolevulinic Acid, Urine
Fabry Disease (GLA) Gene Mutation Analysis
Cortisol/Cortisone, Free, 24 Hour, Urine
Lysozyme (Muramidase), Serum
Tricyclic Antidepressant (TCA), Urine
Hepatitis B Core Antibody, IgM
ASXL3 Gene Mutation Analysis
Allergen Specific IgE, Mold (Allergens) Panel
von Willebrand Disease 2N (Subtype Normandy), Genotyping
Mitochondrial M2 Antibody, IgG

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LDS
/Medical Tests
/1p36.3 Microdeletion Syndrome, FISH

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

1p36.3 Microdeletion Syndrome, FISH
Medical Test

Additional ICD10

Access to 1p36.3 Microdeletion Syndrome, FISH is restricted.