InnovaRx Innova Health Strategies

Pricing Sign in

Q93.89

Other deletions from the autosomes

Billable FY2026 2025-10-01 → 2026-09-30

Exclusions 1 never code together

Excludes2

mitochondrial metabolic disorders (E88.4-)E88.4-

Excludes2 — not included here, but the patient may have both. Code both when documented.

Instructional notes 3

Inclusion terms

Deletions identified by fluorescence in situ hybridization (FISH)
Deletions identified by in situ hybridization (ISH)
Deletions seen only at prometaphase

Index entries leading here 3

Deletion (s)
- autosome Q93.9
  - identified by in situ hybridization (ISH) Q93.89
  - identified by fluorescence in situ hybridization (FISH) Q93.89
- chromosome
  - specified NEC Q93.89
  - seen only at prometaphase Q93.89
- long arm chromosome 18 or 21 Q93.89
Syndrome — see also Disease
- long arm 18 or 21 deletion Q93.89
Monosomy Q93.9
- specified NEC Q93.89

Alongside this code 3 same parent — Q93.8

Q93.81 Velo-cardio-facial syndrome Q93.82 Williams syndrome Q93.88 Other microdeletions

Additional references

AHA Coding Clinic® Licence required

Official coding advice for this code. Published by the American Hospital Association. Not included in this installation.

This code

Billable: yes
Code set: FY2026
Parent: Q93.8
Block: Q90-Q99
Siblings: 3

Present FY2024–FY2027.