- Unknown type - GTR - NCBI

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Unknown type

offered by

GTR Test Accession:

Last updated in GTR:

At a Glance

Conditions (4):

Peroxisome biogenesis disorders, Zellweger syndrome spectrum; Adrenoleukodystrophy; Bifunctional peroxisomal enzyme deficiency more...

Analytes (1):

C26:0-lysophosphatidylcholine

Conditions

Total conditions: 4

Condition/Phenotype	Identifier

Methodology

Total methods: 0

Method Category

Test method

Instrument *

* Instrument: Not provided

Technical Information

Recommended fields not provided:

Test Confirmation

Additional Information

Reviews:

PubMed Clinical Queries

Reviews in PubMed

Clinical resources:

Clinicaltrials.gov

Molecular resources:

View PEX6 variations in ClinVar

View PEX12 variations in ClinVar

View PEX16 variations in ClinVar

Practice guidelines:

ACMG Algorithm, 2023

Consumer resources:

Genetic Alliance

MedlinePlusGenetics (GHR)

NCATS Office of Rare Diseases Research (GARD)

IMPORTANT NOTE: NIH does not independently verify information submitted to GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in 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.