Cytochrome P450 21A2 (CYP21A2) Genotyping
von Willebrand Disease 2N (Subtype Normandy), Genotyping
Acute bronchitis
Autoinflammatory Syndromes (VEXAS syndrome)
Sperm Antibody, IgA and IgG
Porphobilinogen, Urine
Gardnerella vaginalis
Mitochondrial Fission Factor (MFF) Gene Mutation Analysis
Coccidioides By Molecular Method, Body Fluid
Cyclospora Stain
LDS
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Tangier disease (Familial alpha-lipoprotein deficiency)
All
Medical Tests
ICD10
Additional ICD10
SNOMED
All
Medical Tests
ICD10
Additional ICD10
SNOMED
Tangier disease (Familial alpha-lipoprotein deficiency)
Disease
Medical Tests (18)
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