Test ID: FKAL
Kallmann Syndrome, Xp22.3 Deletion, FISH
Secondary ID 
A test code used for billing and in test definitions created prior to November 2011
88540
Useful For Suggests clinical disorders or settings where the test may be helpful
Aiding in the diagnosis of Kallmann syndrome, in conjunction with conventional chromosome studies (#8696 Chromosome Analysis, for Congenital Disorders, Blood)
Detecting cryptic translocations involving Xp22.3 that are not demonstrated by conventional chromosome studies
Special Instructions and Forms Describes specimen collection and preparation information, test algorithms, and other information pertinent to test. Also includes pertinent information and consent forms to be used when requesting a particular test
Method Name A short description of the method used to perform the test
Fluorescence In Situ Hybridization (FISH)
Reporting Name A shorter/abbreviated version of the Published Name for a test; an abbreviated test name
Kallmann, Xp22.3, FISH
Aliases Lists additional common names for a test, as an aid in searching
FISH
FISH (Fluorescent In Situ Hybridization)
Kallman Syndrome
Kallmann Syndrome
Kalman Syndrome
Xp Deletion
Xp22.3
FISH (Fluorescent In Situ Hybridization)
Kallman Syndrome
Kallmann Syndrome
Kalman Syndrome
Xp Deletion
Xp22.3
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