Coma
Williams Syndrome, 7q11.23 Deletion, FISH, Blood
Isocitrate Dehydrogenase 1 (IDH1) Mutation Analysis
Factor XIII, Qualitative, with Reflex to Factor XIII 1:1 Mix
Tobramycin, Serum
Psoriatic arthritis
Glycogen storage disease type II (Pompe disease)
Peripheral neuropathy
Neuroendocrine Neoplasms (Carcinoid Tumors)
Iron, Serum
LDS
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Mucopolysaccharidosis III, Gene Mutation Panel
All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
ICD10
Additional ICD10
References
All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
ICD10
Additional ICD10
References
Mucopolysaccharidosis III, Gene Mutation Panel
Medical Test
Interpretation
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Mucopolysaccharidosis III, Gene Mutation Panel
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