Hereditary Hemolytic Anemia Gene Mutation Panel, NGS
Glanzmann thrombasthenia (hereditary familial thrombocytopenia)
Metabolic alkalosis
Biopsy, Frozen Section
Obstetric Panel
Trypanosoma cruzi (T. cruzi) Antibody, IgG and IgM
Calcium, Serum
Creatinine with Estimated eGFR, Serum
Herpesvirus 7 (HHV-7) Antibody, IgG, IgM
Proteomic Blood Test for Non-Small Cell Lung Cancer (NSCLC), VeriStrat
LDS
Sign up
Log in
LDS
/
Medical Tests
/
Solute Carrier Family 22 (SLC22A5) Gene Mutation 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
Solute Carrier Family 22 (SLC22A5) Gene Mutation Analysis
Medical Test
Reference Ranges
Access to
Solute Carrier Family 22 (SLC22A5) Gene Mutation Analysis
is restricted.
Sign up now