Familial Mediterranean Fever (MEFV) Gene Mutation Analysis
Homovanillic Acid (HVA), Random, Urine
Multiple Sulfatase Deficiency, Gene Mutation Analysis
Candida Species, PCR
Urea Nitrogen (BUN), 24 Hour, Urine
Iron Binding Capacity
Cardiac Fibrinogen, Plasma
Multiple Sclerosis Panel
Factor IX Gene Gene Mutation Analysis
Lactate, CSF

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/Medical Tests
/Kallmann Syndrome, Xp22.3 Deletion, 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

Kallmann Syndrome, Xp22.3 Deletion, FISH
Medical Test

Additional Testing

Access to Kallmann Syndrome, Xp22.3 Deletion, FISH is restricted.