Noonan Spectrum Disorders Gene Mutation Panel, NGS
Erythropoietin
Lactate, Serum
Biopsy, Gallbladder (Cholecystectomy)
Amikacin, Random, Serum
AFF2 (AF4/FMR2 family, member 2) Gene Mutation Analysis
TNF receptor superfamily member 13B Gene Mutation Analysis
Prolyl Hydroxylase Domain-2 (PHD2/EGLN1) Gene Mutation Analysis
Group A Streptococcus (Streptococcus pyogenes), Culture
Isoagglutinin Titer, Anti-B, Serum

LDS
Sign up
Log in

LDS
/Medical Tests
/Genetic Testing for Severe Inherited Diseases, NGS

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

Genetic Testing for Severe Inherited Diseases, NGS
Medical Test

Specimen Collection

Access to Genetic Testing for Severe Inherited Diseases, NGS is restricted.