Prolyl Hydroxylase Domain-2 (PHD2/EGLN1) Gene Mutation Analysis
Sodium, 24 Hour, Urine
Fabry (Anderson) disease
Familial Hypercholesterolemia and Related Diseases Multi-Gene Panel, NGS
Lamellar Body Count, Amniotic Fluid
B-Cell Acute Lymphoblastic Leukemia (ALL), FISH, Blood
Familial dysautonomia
UBE3A Gene Mutation Analysis, Angelman Syndrome, Tissue
Gram Stain, Routine
Cancer Antigen (CA) 19-9, Serum

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LDS
/Medical Tests
/Alpha 1 Antitrypsin Genotyping/Phenotyping

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

Alpha 1 Antitrypsin Genotyping/Phenotyping
Medical Test

Reference Ranges

Access to Alpha 1 Antitrypsin Genotyping/Phenotyping is restricted.