Q93.89 - Other deletions from the autosomes
- Applicable to Other deletions from the autosomes
- The 2026 edition of ICD10-CM Q93.89 became effective on October 1, 2025.
- This is the American ICD10-CM version of Q93.89 - other international versions of ICD10 Q93.89 may differ.
- Q93.89 is a Billable / Specific ICD10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
Inclusion terms help to clarify and specify the conditions or diseases covered by a particular ICD-10-CM code.
Inclusion Term:
- Deletions identified by fluorescence in situ hybridization (FISH)
- Deletions identified by in situ hybridization (ISH)
- Deletions seen only at prometaphase
Billable/Specific Code
The following codes above Q93.89 contain annotation back-references that may be applicable to Q93.89:
- Chapter: Q00-QA0 - Congenital malformations, deformations, chromosomal abnormalities, and genetic disorders
- Section: Q90-Q99 - Chromosomal abnormalities, not elsewhere classified
- Category: Q93 - Monosomies and deletions from the autosomes, not elsewhere classified
Browse other similar CM codes:
Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.
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