von Willebrand Disease 2N (Subtype Normandy), Genotyping
Candida albicans, Antigen
Cancer Antigen (CA) 19-9, Peritoneal Fluid
22q11.2 deletion syndrome
Secretin, Urine
Hypopituitarism
Subtelomeric Region Anomalies, FISH, Blood
Acne vulgaris
Medullary thyroid carcinoma
Seizure disorder
LDS
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Congenital hypothyroidism
All
Medical Tests
ICD10
Additional ICD10
SNOMED
All
Medical Tests
ICD10
Additional ICD10
SNOMED
Congenital hypothyroidism
Disease
Medical Tests (19)
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Congenital hypothyroidism
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ICD10
Access to
Congenital hypothyroidism
is restricted.
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Additional ICD10
Access to
Congenital hypothyroidism
is restricted.
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SNOMED
Access to
Congenital hypothyroidism
is restricted.
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