Wilson Disease, (ATP7B) Gene Mutation Analysis
Measles (Rubeola) Virus Culture
Catechol-O-methyltransferase Genotyping (COMT)
Dextromethorphan, Urine
Alpha 1 Antitrypsin, Fecal
Scarlet fever
Reticulin Antibody, IgA
Aldosterone, Serum
Basic Metabolic Panel (BMP)
Alpha-tropomysin (TPM1) Mutation Analysis
LDS
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21-hydroxylase deficiency
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Medical Tests
ICD10
Additional ICD10
SNOMED
All
Medical Tests
ICD10
Additional ICD10
SNOMED
21-hydroxylase deficiency
Disease
Medical Tests (20)
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21-hydroxylase deficiency
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ICD10
Access to
21-hydroxylase deficiency
is restricted.
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Additional ICD10
Access to
21-hydroxylase deficiency
is restricted.
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SNOMED
Access to
21-hydroxylase deficiency
is restricted.
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