GRACILE Syndrome
Gram Stain, Routine
AFF2 (AF4/FMR2 family, member 2) Gene Mutation Analysis
Electrophoresis, Protein, Serum
Polycystic Kidney Disease, Autosomal Dominant (PKD1 and PKD2), Gene Analysis
Tissue Transglutaminase (tTG) Antibody, IgA
Myeloid Differentiation Primary Response 88 (MYD88) Gene Mutation Analysis
Beta-2 Glycoprotein 1 Antibody, IgG
USP6 (17p13), Aneurysmal Bone Cyst and Nodular Fasciitis, FISH
Haloperidol, Urine
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 Testing
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Hereditary Hemorrhagic Telangiectasia, ENG Gene Mutation Analysis
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