Congenital hypothyroidism
Malignant neoplasm, colon
Acute tubular necrosis
Prostatitis, chronic
Chronic pancreatitis
Kallmann Syndrome, Xp22.3 Deletion, FISH
NOP10 Gene Mutation Analysis
Neuron-Specific Enolase (NSE), Serum
Bone Morphogenetic Protein Receptor Type 1A (BMPR1A) Gene Mutation Analysis
Clomipramine, Urine
LDS
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Scleroderma Associated Antibody (Scl-70), IgG
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
Scleroderma Associated Antibody (Scl-70), IgG
Medical Test
Methodology
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Scleroderma Associated Antibody (Scl-70), IgG
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