- 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:

At a Glance

Conditions (27):

Afibrinogenemia, congenital; Antithrombin III deficiency; Combined deficiency of factor V and factor VIII, 1 more...

Genes (17):

F10 (13q34); F11 (4q35.2); F12 (5q35.3); F13A1 (6p25.1); F2 (11p11.2) more...

Conditions

Total conditions: 27

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 FGA variations in ClinVar

View FGB variations in ClinVar

View FGG 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.