758.9 Alberta AHCIP code: Conditions due to anomaly of unspecified chromosome
758.9 is the Alberta diagnostic code for “Conditions due to anomaly of unspecified chromosome” in Alberta Health’s January 2018 release, in effect from Jan 18, 2018.
Official description
758.9Conditions due to anomaly of unspecified chromosome
Alberta AHCIP diagnostic codes (ICD-9) · Alberta
Notes for 758.9
Alberta Health’s list gives no includes, excludes or other notes for 758.9 or the headings above it.
Where 758.9 sits
- 1ChapterXIV. Congenital anomalies
- 2Valid code 758Chromosomal anomalies
- 3Valid code 758.9Conditions due to anomaly of unspecified chromosome
Source and release
- Data release
- Alberta AHCIP · January 2018
- Effective date
- Jan 18, 2018
- Publisher
- Alberta Health
This page is built from the Alberta AHCIP catalog that Vero Codes reads when it suggests codes: Alberta Health’s January 2018 release, imported from the publisher’s file and checked against it. The description, notes and structured data come from the same record.
Frequently asked questions
What does Alberta diagnostic code 758.9 mean?
758.9 is the Alberta diagnostic code for “Conditions due to anomaly of unspecified chromosome” in Alberta Health’s Alberta AHCIP January 2018 release.
Where is 758.9 in Alberta AHCIP?
758.9 sits under 758 Chromosomal anomalies, within XIV. Congenital anomalies.
What coding notes apply to 758.9?
Alberta Health’s list gives no includes, excludes or other notes for 758.9 or the headings above it.
Which Alberta AHCIP release does this page use?
It uses Alberta Health’s January 2018 release, in effect from Jan 18, 2018. It is a reference: confirm the code against the current list and the payer’s rules before you submit it.
Codes beside 758.9
View 758758.0Chromosomal anomalies – Down's syndrome758.1Chromosomal anomalies – Patau's syndrome758.2Chromosomal anomalies – Edward's syndrome758.3Chromosomal anomalies – Autosomal deletion syndromes758.4Chromosomal anomalies – Balanced autosomal translocation in normal individual758.5Other conditions due to autosomal anomalies758.6Chromosomal anomalies – Gonadal dysgenesis758.7Chromosomal anomalies – Klinefelter's syndrome758.8Other conditions due to sex chromosome anomalies