Medicare Benefits Schedule - Item 73353

Search Results for Item 73353

Category 6 - PATHOLOGY SERVICES

73353

73353 - Additional Information

Item Start Date:
01-May-2020
Description Updated:
01-May-2020
Schedule Fee Updated:
01-May-2020

Group
P7 - Genetics

Detection of a familial mutation for a patient who has a first- or second-degree relative with a documented pathogenic germline gene variant for familial hypercholesterolaemia

Applicable only once per lifetime

Fee: $400.00 Benefit: 75% = $300.00 85% = $340.00


Legend

  • Assist - Addition/Deletion of (Assist.)
  • Amend - Amended Description
  • Anaes - Anaesthetic Values Amended
  • Emsn - EMSN Change
  • Fee - Fee Amended
  • Renum - Item Number Change (renumbered)
  • New - New Item
  • NewMin - New Item (previous Ministerial Determination)
  • Qfe - QFE Change