Kallmann Syndrome, Xp22.3 Deletion, FISH
Gastrointestinal Viral Pathogen Panel, Molecular
Lactate, CSF
Crystal Identification, Synovial Fluid
Aluminum, Random, Urine
Phencyclidine (PCP), Serum
HER2/neu (ERBB2), IHC, Semi Quantitative, Automated
Genetic Testing for Severe Inherited Diseases, NGS
TINF2 Gene Mutation Analysis
Calcium/Creatinine, 24 Hour, Urine
LDS
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Porphobilinogen, Quantitative, Random, Urine
All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Additional Testing
Turnaround Time
CPT
LOINC
ICD10
Additional ICD10
References
All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Additional Testing
Turnaround Time
CPT
LOINC
ICD10
Additional ICD10
References
Porphobilinogen, Quantitative, Random, Urine
Medical Test
Additional ICD10
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Porphobilinogen, Quantitative, Random, Urine
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