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Unknown type

offered by

GTR Test Accession:

Last updated in GTR:

At a Glance

Conditions (63):

Bardet-Biedl syndrome; Adolescent nephronophthisis; Asphyxiating thoracic dystrophy 4 more...

Genes (39):

AHI1 (6q23.3); ARL13B (3q11.1-11.2); ARL6 (3q11.2); B9D1 (17p11.2); B9D2 (19q13.2) more...

Conditions

Total conditions: 63

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 BBS1 variations in ClinVar

View BBS4 variations in ClinVar

View MKKS variations in ClinVar

View SDCCAG8 variations in ClinVar

Practice guidelines:

EuroGentest, 2010

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.