Intact N-Terminal Propeptide of Type 1 Procollagen
9p21 Genotype (CVD Risk Genotype Test)
Acid Phosphatase, Total, Serum
Vitamin D, 25-Hydroxy, fractions (D2 and D3)
Beta-2 Transferrin, CSF
Malignant neoplasm, brain
Kidney transplantation
Oxalate, Plasma
SARS-CoV-2 Coronavirus infection (COVID-19)
Glutamic Acid Decarboxylase (GAD65) Antibody, CSF
LDS
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Congenital hypothyroidism
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Medical Tests
ICD10
Additional ICD10
SNOMED
All
Medical Tests
ICD10
Additional ICD10
SNOMED
Congenital hypothyroidism
Disease
SNOMED
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Congenital hypothyroidism
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