Eosinophil Cationic Protein
Mycoplasma pneumoniae Antibody, IgG
Carnitine Palmitoyltransferase II Deficiency, Gene Mutation Analysis
Mitochondrial M2 Antibody, IgG
Norovirus, EIA, Stool
Neurofibromatosis type 2
PPOX Gene Mutation Analysis, Tissue
Biopsy, Bone
Pernicious anemia
Hydroxyzine, Urine
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
Additional ICD10
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Congenital hypothyroidism
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