Brugada Syndrome Multi-Gene Panel, NGS
Epidermal Nerve Fiber Density (ENFD)
ATM/C11orf65 Gene Variation
Hemoglobin A1c
Amiodarone, Serum
Cryptogenic cirrhosis
WRAP53 Gene Mutation Analysis
Lipoprotein Associated Phospholipase A2 Activity
Fibrinogen Antigen
Chromosome Analysis, for Congenital Disorders, Blood
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Inherited Copper Deficiency (Menkes Syndrome)
All
Medical Tests
ICD10
Additional ICD10
SNOMED
All
Medical Tests
ICD10
Additional ICD10
SNOMED
Inherited Copper Deficiency (Menkes Syndrome)
Disease
Medical Tests (18)
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Inherited Copper Deficiency (Menkes Syndrome)
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ICD10
Access to
Inherited Copper Deficiency (Menkes Syndrome)
is restricted.
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Additional ICD10
Access to
Inherited Copper Deficiency (Menkes Syndrome)
is restricted.
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SNOMED
Access to
Inherited Copper Deficiency (Menkes Syndrome)
is restricted.
Sign up now