Prenatal (Obstetrics) Carrier Screening for Inherited Genetic Conditions (Genesys Carrier Panel, LabCorp Inheritest®, UNITY Fetal Risk screen)
Acetylcholinesterase (AChE), Amniotic Fluid
Diphenhydramine, Urine
Biopsy, Different Sites
Alpha Fetoprotein (AFP), Tumor Marker, Serum/Plasam
5-hydroxytryptamine receptor 1A (HTR1A)
HBB (Hemoglobin, Subunit Beta) Gene Mutation Analysis
DKC1 Gene Mutation Analysis
Polyoma BK Virus, PCR, Qualitative, Urine
Acanthamoeba and Naegleria Culture and Stains, Corneal Scraping
LDS
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TNF receptor superfamily member 13B 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
TNF receptor superfamily member 13B Gene Mutation Analysis
Medical Test
CPT
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TNF receptor superfamily member 13B Gene Mutation Analysis
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