Hepatic coma
Glycogen storage disease type II (Pompe disease)
Williams Syndrome, 7q11.23 Deletion, FISH, CV
Beta-2 Glycoprotein 1 Antibody, IgM
PML-RARA (Promyelocytic Leukemia/Retinoic Acid Receptor Alpha) Translocation, t(15;17) Analysis
Lead, Blood
PAX2, Immunohistochemistry, Tissue
Ehrlichia Antibody, Western Blot
Hemoglobin A1c
Cytomegalovirus (CMV) Antibody, IgG
LDS
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Porphobilinogen, Urine
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Clinical Utility
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Additional Testing
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CPT
LOINC
ICD10
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All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
LOINC
ICD10
Additional ICD10
References
Porphobilinogen, Urine
Medical Test
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