AIRE gene mutation
Carnitine Palmitoyltransferase II Deficiency, Gene Mutation Analysis
Pepsin A
Hemoglobin Electrophoresis
Post-acute COVID-19 Syndrome (PACS)
Microsatellite Instability (MSI), HNPCC/Lynch Syndrome
Rhesus D (Rh D), Typing
Williams Syndrome, 7q11.23 Deletion, FISH, Amniotic Fluid
Cellulitis (skin infection)
Vibrio infection including gastroenteritis

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/Medical Tests
/Microsomal epoxide hydrolase 1 (EPHX1) Gene Variation

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

Microsomal epoxide hydrolase 1 (EPHX1) Gene Variation
Medical Test

Access to Microsomal epoxide hydrolase 1 (EPHX1) Gene Variation is restricted.