Macroamylase
Atherosclerosis of aorta
Comprehensive Pharmacogenetics (PGx) Gene Variation Panel
Acute coronary syndrome
Glomerulonephritis, unspecified
Lynch Syndrome Multi Gene Panel (MLH1, MSH2, MSH6, PMS2 and EPCAM), Genomic Unity®
Thyroiditis
Congestive heart failure
Salla disease (free sialic acid storage disease)
Hepatic steatosis (fatty liver)

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/Tumor Suppressor Gene P53 (TP53) 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

Tumor Suppressor Gene P53 (TP53) Gene Mutation Analysis
Medical Test

Clinical Utility

Access to Tumor Suppressor Gene P53 (TP53) Gene Mutation Analysis is restricted.

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