Mucopolysaccharidosis type II (Hunter Syndrome)
Protein S, Functional
Congenital hemolytic anemia
Hypoglycemia
Extractable Nuclear Antigen Antibody Panel (Autoantibodies in Connective Tissue Diseases)
Urinary incontinence in men
Nocardia Stain
Systemic mastocytosis
Delayed puberty (male and female)
Beta-amyloid Protein Ratio 1-42/1-40 (QUEST AD-Detect™, INNOTEST® B-AMYLOID), Plasma
LDS
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Myotonic dystrophy
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ICD10
Additional ICD10
SNOMED
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Medical Tests
ICD10
Additional ICD10
SNOMED
Myotonic dystrophy
Disease
ICD10
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