PTPN11 Gene Mutation Analysis for Noonan Syndrome
Hyperkalemia
Glomerular Basement Membrane Antibody, IgG
Anaplastic Lymphoma Kinase (ALK) Gene Mutation Analysis
Carbon monoxide poisoning
Tapentadol, Urine
Mycoplasma pneumoniae Antibody, CF (CSF)
Weaver syndrome
MDA, Urine
Ethosuximide, Serum
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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
Medical Tests (20)
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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.
Sign up now