Multiple Sulfatase Deficiency, Gene Mutation Analysis
Solute Carrier Family 28 Member 3 (SLC28A3) Genotyping
Electrophoresis, Protein, 24 Hour, Urine
CDKN1C Gene Mutation Analysis
Beta-2 Glycoprotein 1 Antibody, IgG

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/17-Hydroxypregnenolone, Serum

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

17-Hydroxypregnenolone, Serum
Medical Test

Additional ICD10

Access to 17-Hydroxypregnenolone, Serum is restricted.

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