Chlamydia Pneumoniae, Molecular
Prenatal (Obstetrics) Carrier Screening for Inherited Genetic Conditions (Genesys Carrier Panel, LabCorp Inheritest®, UNITY Fetal Risk screen)
Amylase, Random, Urine
Parvovirus B19 Antibody, IgG and IgM
Cryptococcus Antigen, Spinal Fluid
Aldosterone, Urine
LDL Subclasses
Streptococcus pneumoniae, Molecular
Clostridium difficile (C. Diff), Culture
Olanzapine, Urine or Serum
LDS
Sign up
Log in
LDS
/
Medical Tests
/
Spinocerebellar Ataxia Type 1 (ATXN1) Gene Mutation Analysis
All
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
Spinocerebellar Ataxia Type 1 (ATXN1) Gene Mutation Analysis
Medical Test
References
Access to
Spinocerebellar Ataxia Type 1 (ATXN1) Gene Mutation Analysis
is restricted.
Sign up now
Loading...