Alprazolam, Urine
Prader-Willi syndrome
Transthyretin (TTR) Gene Mutation Analysis
CACNA1A (calcium voltage-gated channel subunit alpha1 A) Gene Mutation Analysis
5'-Nucleotidase
Hereditary Colon Cancer Gene Mutation Panel (Lynch syndrome), NGS
Viral gastroenteritis due to Rotavirus
OncobiotaLUNG for Lung Cancer Diagnosis
HLA DQ Genotyping for Celiac Disease
Phosphatidylserine Antibody, IgA, IgM, IgG
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21-hydroxylase deficiency
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Medical Tests
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Additional ICD10
SNOMED
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Medical Tests
ICD10
Additional ICD10
SNOMED
21-hydroxylase deficiency
Disease
Additional ICD10
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21-hydroxylase deficiency
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