- Unknown type - GTR - NCBI

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Unknown type

offered by

GTR Test Accession:

Last updated in GTR:

At a Glance

Conditions (24):

Retinitis pigmentosa 39; Deafness, autosomal dominant 11; Deafness, autosomal recessive 12 more...

Genes (14):

ABHD12 (20p11.21); ADGRV1 (5q14.3); CDH23 (10q22.1); CEP250 (20q11.22); CIB2 (15q25.1) more...

Conditions

Total conditions: 24

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 USH2A variations in ClinVar

Coriell Institute for Medical Research

Consumer resources:

Genetic Alliance

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.