Malignant neoplasm, colon
Acute tubular necrosis
Prostatitis, chronic
Chronic pancreatitis
Kallmann Syndrome, Xp22.3 Deletion, FISH
NOP10 Gene Mutation Analysis
Neuron-Specific Enolase (NSE), Serum
Bone Morphogenetic Protein Receptor Type 1A (BMPR1A) Gene Mutation Analysis
Clomipramine, Urine
Biopsy, Gallbladder (Cholecystectomy)
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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