Gastrointestinal Viral Pathogen Panel, Molecular
Lactate, CSF
Crystal Identification, Synovial Fluid
Aluminum, Random, Urine
Phencyclidine (PCP), Serum
HER2/neu (ERBB2), IHC, Semi Quantitative, Automated
Genetic Testing for Severe Inherited Diseases, NGS
TINF2 Gene Mutation Analysis
Calcium/Creatinine, 24 Hour, Urine

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LDS
/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

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