Pregnenolone
Williams Syndrome, 7q11.23 Deletion, FISH, Tissue
Soluble Fibrin Monomer
Diphenhydramine, Urine
IgG Subclasses
Peripheral Myelin Protein 22 (PMP22), Peripheral Neuropathy, FISH
Protein, Total, Serum
Blastomyces Antibody, Spinal Fluid
Inhibin A and B, Tumor Marker
14-3-3 Protein Tau/Theta, Spinal Fluid

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/Medical Tests
/Hereditary Hemolytic Anemia Gene Mutation Panel, NGS

All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
ICD10
Additional ICD10
References

All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
ICD10
Additional ICD10
References

Hereditary Hemolytic Anemia Gene Mutation Panel, NGS
Medical Test

Additional ICD10

Access to Hereditary Hemolytic Anemia Gene Mutation Panel, NGS is restricted.