Medicare Benefits Schedule - Item 73363

Search Results for Item 73363



73363 - Additional Information

Item Start Date:
Description Updated:
Schedule Fee Updated:

P7 - Genetics

Testing of a person (the person tested) for the detection of a single gene variant for segregation analysis in relation to another person (the patient), if:

  1. the patient has a known phenotype of a suspected monogenic condition; and
  2. a service described in item 73358 or 73360 has identified a potentially causative variant for the patient; and
  3. the person tested is a biological parent or other biological relative of the patient; and
  4. a sample from the person tested has not previously been tested in relation to the patient for a service to which item 73359 applies; and
  5. the results of the testing of the person tested for this service are made available for the purpose of providing the detection for the patient; and
  6. the detection is:
    1. requested by a consultant physician practising as a clinical geneticist; or
    2. requested by a consultant physician practising as a specialist paediatrician, following consultation with a clinical geneticist; and
  7. the detection is not performed in conjunction with item 73361 or 73362

Applicable only once per variant per lifetime

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


  • 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