• Osmolality, Body Fluid
  • Aldosterone/Renin Activity Ratio
  • Complement Component C4
  • Bacterial Culture, Anaerobic
  • Antithrombin Activity
  • Amphetamines/Sympathomimetic Amines, Urine
  • Adenovirus, Viral Culture
  • Tangier disease (Familial alpha-lipoprotein deficiency)
  • Prenatal Carrier Screening for Inherited Genetic Conditions (Genesys Carrier Panel, LabCorp Inheritest®, UNITY Fetal Risk screen)
  • Carbamazepine, Free, Serum
  • LDS
  • Sign up
  • Log in
  • LDS
  • /Medical Tests
  • /X-linked Intellectual Disability Gene Mutation Panel, NGS
  • 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

X-linked Intellectual Disability Gene Mutation Panel, NGS
Medical Test

Clinical Utility
Access to X-linked Intellectual Disability Gene Mutation Panel, NGS is restricted.