Thyroid Stimulating Hormone (TSH)
Lower gastrointestinal hemorrhage
Stillbirth
Glomerulonephritis, chronic
Pleural effusion
Behçet’s disease (Behcet syndrome)
Norfentanyl, Urine
Hypochondroplasia (FGFR3) Gene Mutation Analysis
Immunoglobulin G/Albumin Ratio, CSF
Methylation Cancer Marker Detection in Cell-free Circulating Tumor DNA (Northstar Select and Response™)

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LDS
/Medical Tests
/Hypochondroplasia (FGFR3) Gene 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

Hypochondroplasia (FGFR3) Gene Mutation Analysis
Medical Test

Clinical Utility

Access to Hypochondroplasia (FGFR3) Gene Mutation Analysis is restricted.