Aortic Dysfunction or Dilation (eg, Marfan syndrome, Loeys Dietz syndrome, Ehler Danlos syndrome type IV, arterial tortuosity syndrome) Gene Mutation Panel, NGS
Oxycodone, Serum
Dengue Virus Antibody, IgG, Serum
Bone Morphogenetic Protein Receptor Type 1A (BMPR1A) Gene Mutation Analysis
Bacterial Vaginosis Pathogens by Molecular Method
Neurofibromatosis Type 1 (NF1) Gene Mutation Analysis
Opioid-use Disorder Pain Management Genotyping Panel
Drug Testing, Presumptive (Drug Screen), Urine
Urinary pH
1p/19q Deletion in Gliomas, FISH, Tissue

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LDS
/Medical Tests
/FBN1 (Fibrillin-1) Genetic 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

FBN1 (Fibrillin-1) Genetic Mutation Analysis
Medical Test

Access to FBN1 (Fibrillin-1) Genetic Mutation Analysis is restricted.