Rare Constitutional and hereditary Diseases, Whole Exome Sequence Analysis, NGS
Methamphetamine, Urine
Immunoglobulin Subclass IgG4
B-Cell Acute Lymphoblastic Leukemia (ALL), FISH, Bone Marrow
VDRL, Serum
Legionella pneumophila Antibody, IgM by IFA
Minimal Residual Disease (MRD) for Early Detection of Cancer Recurrence (Signatera™, Haystack MRD™)
Chikungunya Virus RNA, Real-Time PCR, Qualitative
UBE3A Gene Mutation Analysis, Angelman Syndrome, Blood
Doxepin, Urine
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Sphingomyelin Phosphodiesterase 1 (SMPD1) Mutation Analysis, Niemann-Pick Disease
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Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
LOINC
ICD10
Additional ICD10
References
All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
LOINC
ICD10
Additional ICD10
References
Sphingomyelin Phosphodiesterase 1 (SMPD1) Mutation Analysis, Niemann-Pick Disease
Medical Test
ICD10
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Sphingomyelin Phosphodiesterase 1 (SMPD1) Mutation Analysis, Niemann-Pick Disease
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