Other deletions from the autosomes
Billable / specificPOA exempt
Q93.89 is a billable, specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes in FY2027.
Inclusion terms
Applicable to
- Deletions identified by fluorescence in situ hybridization (FISH)
- Deletions identified by in situ hybridization (ISH)
- Deletions seen only at prometaphase
Includes (from Q93)
- Note: Codes from this chapter are not for use on maternal records
Excludes2
Not included here — may be reported together when both conditions exist.
Also known as
- Deletions identified by fluorescence in situ hybridization (FISH)
- Deletions identified by in situ hybridization (ISH)
- Deletions seen only at prometaphase
- Deletion, autosome, identified by fluorescence in situ hybridization
- Deletion, autosome, identified by in situ hybridization
- Deletion, chromosome, seen only at prometaphase
- Deletion, chromosome, specified NEC
- Deletion, long arm chromosome 18 or 21
- Monosomy, specified NEC
- Syndrome, long arm 18 or 21 deletion
Parent code
- Q93.8Other deletions from the autosomesHeader