- Unknown type - GTR - NCBI

Skip to main page content

Genetic Testing Registry

View Advanced Search Options

Classic view of this page

see more see less

Unknown type

offered by

GTR Test Accession:

Last updated in GTR:

View version history

GTR000506412.12, last updated: 2019-04-15

GTR000506412.11, last updated: 2019-03-20

GTR000506412.10, last updated: 2017-08-25

GTR000506412.9, last updated: 2016-05-13

GTR000506412.8, last updated: 2015-09-01

GTR000506412.7, last updated: 2014-07-07

GTR000506412.6, last updated: 2014-07-02

GTR000506412.5, last updated: 2014-06-17

GTR000506412.4, last updated: 2014-06-13

GTR000506412.3, last updated: 2014-05-30

GTR000506412.2, last updated: 2014-05-05

GTR000506412.1, registered in GTR: 2014-05-05

At a Glance

Conditions (252):

Retinitis pigmentosa 13; 11p partial monosomy syndrome; 3-Methylglutaconic aciduria type 3 more...

Genes (138):

ABCA4 (1p22.1); ADAM9 (8p11.22); AHI1 (6q23.3); AIPL1 (17p13.2); BBS1 (11q13.2) more...

Conditions

Total conditions: 252

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 PRPF8 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.