Acute hepatic failure
Hexosaminidase A (HEXA) Gene Mutation Analysis
TNNC1 (Troponin C) Gene Mutation Analysis
Syphilis, secondary
Amino Acids Quantitative by LC-MS/MS, Plasma
Parathyroid Hormone, Fine-Needle Aspiration Biopsy (FNAB), Needle Wash
Cerebral arterial thrombosis
Galleri Multi-Cancer Early Detection Test
Neurofibromatosis type 2
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Cowden Syndrome
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ICD10
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SNOMED
Cowden Syndrome
Disease
Medical Tests (3)
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Cowden Syndrome
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ICD10
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Cowden Syndrome
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Additional ICD10
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Cowden Syndrome
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SNOMED
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Cowden Syndrome
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