Calcium, 24 Hour, Urine
Myotonic dystrophy
Bartonella Antibody, IgG and IgM, Serum
Gabapentin, Serum
Flunitrazepam, Serum
ADAMTS2 Gene Mutation Analysis
Oligoclonal Bands, CSF
NOP10 Gene Mutation Analysis
Acetylcholinesterase (AChE), Amniotic Fluid
Gastrointestinal Parasite Pathogen Panel, Molecular
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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
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.
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