GTR Test Accession:
Help
Last updated in GTR:
View version history
GTR000575330.3,
last updated:
2024-02-27
GTR000575330.2,
last updated:
2022-02-24
GTR000575330.1,
registered in GTR:
2021-02-25
At a Glance
Conditions (12):
Help
Migraine, familial hemiplegic, 1;
CARASIL syndrome;
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
more...
Genes (4):
Help
ATP1A2 (1q23.2);
CACNA1A (19p13.13);
NOTCH3 (19p13.12);
SCN1A (2q24.3)
Conditions
Help
Total conditions: 12
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:
Practice guidelines:
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.