Prenatal (Obstetrics) Carrier Screening for Inherited Genetic Conditions (Genesys Carrier Panel, LabCorp Inheritest®, UNITY Fetal Risk screen)
11-Dehydro-Thromboxane B2, Urine
Acquired hypothyroidism
AIRE gene mutation
Thyroid Stimulating Hormone (TSH)
Peripheral neuropathy
Giardia Species by PCR, Stool
Secondary hypertension
Biopsy, Cervical
Culture, Dental (Routine)
LDS
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Interferon-γ Receptor (IFNGR1) Deficiency
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
Interferon-γ Receptor (IFNGR1) Deficiency
Medical Test
Additional ICD10
Access to
Interferon-γ Receptor (IFNGR1) Deficiency
is restricted.
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