- Unknown type - GTR - NCBI

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Unknown type

offered by

GTR Test Accession:

Last updated in GTR:

At a Glance

Conditions (33):

Deafness, autosomal recessive 12; Branchiootic syndrome 3; Branchiootorenal syndrome 2 more...

Genes (23):

CDH23 (10q22.1); CLRN1 (3q25.1); DFNB31 (9q32); EYA1 (8q13.3); FOXI1 (5q35.1) more...

Conditions

Total conditions: 33

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 ATP2B2 variations in ClinVar

View CDH23 variations in ClinVar

Coriell Institute for Medical Research

Consumer resources:

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.