- Unknonw type - GTR - NCBI

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Unknonw type

offered by

GTR Test Accession:

Last updated in GTR:

At a Glance

Conditions (1886):

Mowat-Wilson syndrome; 11p partial monosomy syndrome; 3 beta-Hydroxysteroid dehydrogenase deficiency; ...

Genes (1858):

AAAS (12q13.13), AARS1 (16q22.1), AARS2 (6p21.1), AASS (7q31.32), ABAT (16p13.2), ...

Conditions

Total conditions: 1886

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 ZEB2 variations in ClinVar

Coriell Institute for Medical Research

Practice guidelines:

EuroGenetest, 2011

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.