22q11.2 microdeletion (DiGeorge) syndrome
Salla disease
Membranoproliferative glomerulonephritis
Insulinoma
Dyspnea
Periodic Acid-Schiff (PAS), Fungus
CaM Kinase II (CaMKII, Calcium-dependent Calmodulin Protein Kinase II) Activation
Ethosuximide, Urine
MAML2 (11q21) Rearrangement, Mucoepidermoid Carcinoma (MEC), FISH, Tissue
Potassium, Random, Urine

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LDS
/Medical Tests
/Factor XIII (F13A1) V34L Genetic Variation 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

Factor XIII (F13A1) V34L Genetic Variation Analysis
Medical Test

Additional Testing

Access to Factor XIII (F13A1) V34L Genetic Variation Analysis is restricted.