Hereditary Hearing Loss Gene Panel
Complete Blood Cell Count (CBC) with Differential
PDGFRA, Gene Mutation Analysis, Exon 14
Autopsy
Interleukin 1 beta (IL-1β)
Vitamin B3 (Niacin)
Ehrlichia chaffeensis Antibody, IgG
Cardiac arrhythmia
Ataxia Telangiectasia Mutated (ATM)
Pediatric Acute-onset Neuropsychiatric Syndrome (PANS)
LDS
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Mucopolysaccharidosis type I
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Medical Tests
ICD10
Additional ICD10
SNOMED
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Medical Tests
ICD10
Additional ICD10
SNOMED
Mucopolysaccharidosis type I
Disease
ICD10
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Mucopolysaccharidosis type I
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