Category 6 - PATHOLOGY SERVICES
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:
- the person tested has a first‑degree relative (the relative) with a known monogenic condition; and
- a service described in item 73358, 73359 or 73360 has identified the causative variant for the relative’s condition; and
- the results of the testing performed for the relative are made available for the purpose of providing the detection for the person tested; and
- the detection is requested by a consultant physician or specialist; and
- 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