Carbohydrate Deficient Transferrin for Congenital Disorders of Glycosylation, Serum
Phospholipid (Cardiolipin) Antibody Panel, IgA, IgG, IgM
Biopsy, Salivary Gland
Hepatitis C Virus (HCV) NS3/4A Protease Inhibitor Resistance, GenoSure
Calcium, 24 Hour, Urine
Aspergillus (Galactomannan) Antigen, Serum
MLYCD Gene Mutation Analysis, Tissue
Angiotensin Converting Enzyme (ACE), CSF
Protein S, Functional
AIRE gene mutation
LDS
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Hereditary Hemorrhagic Telangiectasia, ENG 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
Hereditary Hemorrhagic Telangiectasia, ENG Gene Mutation Analysis
Medical Test
Additional ICD10
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Hereditary Hemorrhagic Telangiectasia, ENG Gene Mutation Analysis
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