Hypothyroidism
Carbohydrate Deficient Transferrin for Congenital Disorders of Glycosylation, Serum
Bone Morphogenetic Protein Receptor Type 1A (BMPR1A) Gene Mutation Analysis
Triglycerides, Serum
Fine Needle Aspiration, Breast
Vitamin B6 (Pyridoxal Phosphate)
Histoplasma capsulatum Antigen, CSF
ADAMTS2 Gene Mutation Analysis
Survival of Motor Neuron 1 (SMN1) Mutation Analysis
Brain-derived Neurotrophic Factor (BDNF) Genotyping
LDS
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Alpha 1 Antitrypsin Genotyping/Phenotyping
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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
Alpha 1 Antitrypsin Genotyping/Phenotyping
Medical Test
Specimen Collection
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Alpha 1 Antitrypsin Genotyping/Phenotyping
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