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Viewing:  Dec 6, 2019

Tay Sachs Disease, HEXA Gene Mutation Analysis

a.k.a.  HEXA gene mutation analysis, Hexosaminidase A Deficiency DNA assay, GM2 gangliosidosis, type 1, TSD, Sphingolipidosis, Tay-Sachs, HexA deficiency, Hexosaminidase alpha-subunit deficiency (variant B), Tay-Sachs Disease (HEXA), HEXA Gene, Full Gene Analysis, B variant GM2 gangliosidosis, HEXMS, Hexosaminidase A deficiency

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  • diseases the test is often used to detect or monitor
  • specimen collection methods/procedures
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    • ICD-10-CM
    • ICD-9-CM
    • CPT
  • additional or related tests
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  • web resources - additional online information about the test
Access to this feature is available in the following products:
  • Medical Lab Tests w/CLD Ranks

SAMPLE PAGE showing data for:  ABO Group and Rh Typing

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