Ammonia, Serum
Fatty Acids, Free
Usher Syndrome, Types 1F and 3 (PCDH15 and CLRN1), 2 Variants
17-Ketosteroids, Urine
Human T-Cell Lymphotropic Virus (HTLV) I/II Antibody Screen
Vitamin A
Collagen Crosslinked C-telopeptide
Duodenal Mucosal Biopsy, Endoscopic
Bilirubin, Direct, Serum
UDP-glucuronosyl Transferase 1A6 (UGT1A6) Genotyping

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/Medical Tests
/PPOX Gene Mutation Analysis, Tissue

All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
ICD10
Additional ICD10
References

All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
ICD10
Additional ICD10
References

PPOX Gene Mutation Analysis, Tissue
Medical Test

Access to PPOX Gene Mutation Analysis, Tissue is restricted.