Medicare Benefits Schedule - Item 73362

Search Results for Item 73362

Category 6 - PATHOLOGY SERVICES

73362

73362 - Additional Information

Item Start Date:
01-May-2020
Description Updated:
01-Nov-2021
Schedule Fee Updated:
01-May-2020

Group
P7 - Genetics

Testing of a person (the person tested) for the detection of a single gene variant for the purpose of reproductive decision making, if:

  1. the person tested has a first‑degree relative (the relative) with a known monogenic condition; and
  2. a service described in item 73358, 73359 or 73360 has identified the causative variant for the relative’s condition; and
  3. the results of the testing performed for the relative are made available for the purpose of providing the detection for the person tested; and
  4. the detection is requested by a consultant physician or specialist; and
  5. the detection is not performed in conjunction with item 73359, 73361 or 73363

Applicable only once per variant 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