Genetic Testing for Childhood Syndromes

This page provides information on the amendments to the descriptors for three items relating to genetic testing for childhood syndromes from 1 November 2021.

Page last updated: 04 November 2021

From 1 November 2021, amendments will be made to the descriptors of three items relating to genetic testing for childhood syndromes.

These items are:

  • amended item 73361, for genetic analysis of a single gene variant for detection purposes in a person who has a biological sibling with a known monogenic condition,
  • amended item 73362, for genetic analysis of a single gene variant for detection purposes in a person who has a first-degree relative with a known monogenic condition, and
  • amended item 73363, for genetic analysis of a single gene variant for segregation analysis in a person who is a biological parent or biological relative to an individual with a known monogenic condition.

PDF Version Factsheet Genetic testing for childhood syndromes (PDF 83 KB)

Word Version Factsheet Genetic testing for childhood syndromes (Word 183 KB)





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