Prenatal (Obstetrics) Carrier Screening for Inherited Genetic Conditions (Genesys Carrier Panel, LabCorp Inheritest®, UNITY Fetal Risk screen)
von Willebrand Disease 2N (Subtype Normandy), Genotyping
Macroprolactin, Serum
Cyclic AMP, Urine
Heparin Induced Antibody
Uniparental Disomy, FISH, Amniotic Fluid
B-Cell Lymphoma, FISH, Blood
CHIC2, 4q12 Deletion (FIP1L1 and PDGFRA Fusion), FISH, Blood
Alpha-cardiac actin (ACTC1) Mutation Analysis
C-Peptide
LDS
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Fatty Acid Profile, Serum
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
Fatty Acid Profile, Serum
Medical Test
Additional ICD10
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Fatty Acid Profile, Serum
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