Primary myelofibrosis (PMF)
Upper gastrointestinal hemorrhage
Chronic gastritis
Hypereosinophilic syndrome
Essential thrombocythemia
Red Blood Cell Antigen Genotyping (Immucor PreciseType, BLOODchip® ID CORE XT™)
Merkel Cell Carcinoma
Chronic liver disease
Hyperprolactinemia
Crohn's disease

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/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

Additional Testing

Access to Spinocerebellar Ataxia Type 1 (ATXN1) Gene Mutation Analysis is restricted.