Lysoganglioside GM1 Antibody, IgG
Primary ovarian insufficiency
Ghrelin Total, Plasma
Cowden Syndrome
Williams Syndrome, 7q11.23 Deletion, FISH, Blood
Bohring-Opitz syndrome
Testosterone, Bioavailable
Pseudomembranous colitis
Blastomycosis
Lysozyme (Muramidase), Serum

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LDS
/Medical Tests
/Familial Dysautonomia Genetic 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

Familial Dysautonomia Genetic Mutation Analysis
Medical Test

Reference Ranges

Access to Familial Dysautonomia Genetic Mutation Analysis is restricted.