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GTR Home > Tests > X-Linked Intellectual Disability (XLID) Sequencing Panel

Overview

Test order codeHelp: NGS XLID Panel

Test name

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X-Linked Intellectual Disability (XLID) Sequencing Panel

Purpose of the test

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This is a clinical test intended for Help: Diagnosis

Condition

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Click Indication tab for more information.

How to order

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Order URL Help: https://www.ggc.org/test-finder-item/x-linked-intellectual-disability-xlid-114-gene-sequencing-panel

Specimen source

Amniocytes
Amniotic fluid
Cell culture
Chorionic villi
Cord blood
Fibroblasts
Fresh tissue
Isolated DNA
Peripheral (whole) blood
Saliva
Skin

Methodology

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Molecular Genetics
CSequence analysis of the entire coding region
Next-Generation (NGS)/Massively parallel sequencing (MPS)

Summary of what is tested

Click Methodology tab for more information.

Clinical utility

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Not provided

Clinical validity

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Not provided

Test services

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  • Clinical Testing/Confirmation of Mutations Identified Previously
  • Custom Prenatal Testing, comments

Practice guidelines

  • Retired, AAN/CNS, 2011
    Retired: Evidence report: Genetic and metabolic testing on children with global developmental delay: report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society.

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.