Smith (ENA) Antibody, IgG
Porphobilinogen, Urine
Hepatic coma
Glycogen storage disease type II (Pompe disease)
Williams Syndrome, 7q11.23 Deletion, FISH, CV
Beta-2 Glycoprotein 1 Antibody, IgM
PML-RARA (Promyelocytic Leukemia/Retinoic Acid Receptor Alpha) Translocation, t(15;17) Analysis
Lead, Blood
PAX2, Immunohistochemistry, Tissue
Ehrlichia Antibody, Western Blot
LDS
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Familial Mediterranean Fever (MEFV) 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
Familial Mediterranean Fever (MEFV) Gene Mutation Analysis
Medical Test
Additional Testing
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Familial Mediterranean Fever (MEFV) Gene Mutation Analysis
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