TNNI3 (Troponin I) Gene Mutation Analysis
Comprehensive Epilepsy Gene Mutation Panel, NGS
CHIC2, 4q12 Deletion (FIP1L1 and PDGFRA Fusion), FISH, Blood
Hyperthyroidism and other causes of thyrotoxicosis
Helicobacter pylori gastrointestinal tract infection
Beckwith-Wiedemann Syndrome (BWS)/Russell-Silver Syndrome (RSS) Molecular Analysis
Hereditary diffuse gastric cancer
Lecithin-sphingomyelin (L/S) Ratio
Ganciclovir, Serum
Viral hepatitis
LDS
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LDS
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Vitamin C deficiency (Scurvy)
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Medical Tests
ICD10
Additional ICD10
SNOMED
All
Medical Tests
ICD10
Additional ICD10
SNOMED
Vitamin C deficiency (Scurvy)
Disease
ICD10
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Vitamin C deficiency (Scurvy)
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