- Unknown type - GTR - NCBI

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Unknown type

offered by

GTR Test Accession:

Last updated in GTR:

View version history

GTR000522580.13, last updated: 2022-12-06

GTR000522580.12, last updated: 2022-11-22

GTR000522580.11, last updated: 2022-10-20

GTR000522580.10, last updated: 2022-10-13

GTR000522580.9, last updated: 2022-08-25

GTR000522580.8, last updated: 2022-05-02

GTR000522580.7, last updated: 2022-04-28

GTR000522580.6, last updated: 2019-01-15

GTR000522580.5, last updated: 2018-05-18

GTR000522580.4, last updated: 2017-12-11

GTR000522580.3, last updated: 2017-05-16

GTR000522580.2, last updated: 2017-02-09

GTR000522580.1, registered in GTR: 2016-06-16

At a Glance

Conditions (86):

Mucopolysaccharidosis type VII; ALG9 congenital disorder of glycosylation; Aase syndrome more...

Genes (87):

ALG1 (16p13.3); ALG9 (11q23.1); ASAH1 (8p22); BRAF (7q34); CANT1 (17q25.3) more...

Conditions

Total conditions: 86

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 GUSB variations in ClinVar

Coriell Institute for Medical Research

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.