Galactose epimerase deficiency, 230350, Autosomal recessive (Galactosemia) (GALE gene) (Sequence Analysis-All Coding Exons) (Postnatal)
- GTR Test IDHelpEach Test is a specific, orderable test from a particular laboratory, and is assigned a unique GTR accession number. The format is GTR00000001.1, with a leading prefix 'GTR' followed by 8 digits, a period, then 1 or more digits representing the version. When a laboratory updates a registered test, a new version number is assigned.: GTR000584042.1
- Last updated: 2022-05-14
- Annual Review past due read more
- Test version history
- 584042.1, last updated: 2022-05-14
Clinical testHelpIn the U.S., clinical tests must be performed under CLIA certification. When a lab uses the same methods for a test in both clinical and research settings, the test appears as two separate GTR records. for UDPglucose-4-epimerase deficiency
Offered by Intergen
- ACMG Algorithm, 2022American College of Medical Genetics Algorithm, Primary or Secondary Hypergalactosemia (Galactose Elevated)
- ACMG ACT, 2022American College of Medical Genetics and Genomics, Newborn Screening ACT Sheet, Elevated total galactose with normal GALT enzyme activity, Primary or Secondary Hypergalactosemia, 2022
- ACMG ACT, 2022American College of Medical Genetics ACT Sheet, Newborn Screening ACT Sheet Primary or Secondary Hypergalactosemia
- ACMG ACT Sheet, 2010American College of Medical Genetics ACT SHEETs, Primary or Secondary Hypergalactosemia, 2010
- ACMG Algorithm, 2009American College of Medical Genetics Algorithm, Primary or Secondary Hypergalactosemia, 2009
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