GTR Test Accession:
Help
Last updated in GTR:
View version history
GTR000515550.18,
last updated:
2020-09-11
GTR000515550.17,
last updated:
2020-09-09
GTR000515550.16,
last updated:
2018-07-03
GTR000515550.15,
last updated:
2018-06-01
GTR000515550.14,
last updated:
2018-02-22
GTR000515550.13,
last updated:
2017-12-04
GTR000515550.12,
last updated:
2017-01-05
GTR000515550.11,
last updated:
2017-01-03
GTR000515550.10,
last updated:
2016-09-26
GTR000515550.9,
last updated:
2016-07-08
GTR000515550.8,
last updated:
2016-03-30
GTR000515550.7,
last updated:
2016-03-08
GTR000515550.6,
last updated:
2016-01-28
GTR000515550.5,
last updated:
2015-09-18
GTR000515550.4,
last updated:
2015-08-14
GTR000515550.3,
last updated:
2015-02-27
GTR000515550.2,
last updated:
2014-09-12
GTR000515550.1,
registered in GTR:
2014-08-22
At a Glance
Conditions (27):
Help
Cataract and cardiomyopathy;
Adult onset ataxia with oculomotor apraxia;
Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 1
more...
Genes (22):
Help
Conditions
Help
Total conditions: 27
| Condition/Phenotype | Identifier |
|---|
Methodology
Total methods: 0
Method Category
Help
Test method
Help
Instrument *
* Instrument: Not provided
Technical Information
Recommended fields not provided:
Test Confirmation
Additional Information
Clinical resources:
Molecular resources:
Consumer resources:
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.