1p36 deletion (monosomy) syndrome
Estrogen/Progesterone Receptor, IHC, Semi-Quantitative
Friedreich Ataxia, Frataxin, Quantitative, Blood
Culture, Genital
21-Hydroxylase Antibody
Tobramycin, Serum
Comprehensive Mitochondrial Disorders Gene Analysis Panel, NGS (Genomic Unity®)
Vitamin E
Von Hippel-Lindau (VHL) Gene Mutation Analysis
Helicobacter pylori, Urea Breath Test
LDS
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Ferritin
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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
Ferritin
Medical Test
Specimen Collection
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Ferritin
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