Legius Syndrome (SPRED1) Sequencing
Trichinella Antibody, IgG and IgM
Apolipoprotein B (APOB) Mutation Detection
Hepatitis C Virus (HCV) Antibody
Rheumatoid Factor (RF)
Diltiazem, Serum
CSRP3 Gene Mutation Analysis
11-Deoxycortisol, Quantitative, Serum
Methlyenetetrahydrofolate reductase (MTHFR) Mutation Analysis
Basic Metabolic Panel (BMP)
LDS
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Inherited Copper Deficiency (Menkes Syndrome)
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Medical Tests
ICD10
Additional ICD10
SNOMED
All
Medical Tests
ICD10
Additional ICD10
SNOMED
Inherited Copper Deficiency (Menkes Syndrome)
Disease
SNOMED
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Inherited Copper Deficiency (Menkes Syndrome)
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