von Willebrand Disease 2N (Subtype Normandy), Genotyping
Vasculitis, Systemic
Proteomic Blood Test for Non-Small Cell Lung Cancer (NSCLC), VeriStrat
Hyponatremia
Alzheimer's disease
Lysozyme (Muramidase), Serum
Tangier disease (Familial alpha-lipoprotein deficiency)
Maple Syrup Disease Genetic Testing
Peritoneal Fluid Analysis
Syphilis, latent

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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

Reference Ranges

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