Other specified trisomies and partial trisomies of autosomes
Billable / specificPOA exempt
Q92.8 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
- Duplications identified by fluorescence in situ hybridization (FISH)
- Duplications identified by in situ hybridization (ISH)
- Duplications seen only at prometaphase
Includes (from Q92)
- unbalanced translocations and insertions
- Note: Codes from this chapter are not for use on maternal records
Excludes1
Not coded here — never report together with this code.
Excludes2
Not included here — may be reported together when both conditions exist.
Also known as
- Duplications identified by fluorescence in situ hybridization (FISH)
- Duplications identified by in situ hybridization (ISH)
- Duplications seen only at prometaphase
- Accessory, chromosome, with complex rearrangements NEC, seen only at prometaphase
- Cat, eye syndrome
- Duplication, duplex, chromosome NEC, seen only at prometaphase
- Syndrome, cat eye
- Syndrome, trisomy, 20
- Syndrome, trisomy, 22
- Trisomy, chromosome specified NEC
- Trisomy, chromosome specified NEC, specified NEC
- Trisomy, specified NEC
- Trisomy, whole chromosome, specified NEC
- Trisomy, 20
- Trisomy, 22
Parent code
- Q92Other trisomies and partial trisomies of the autosomes, not elsewhere classifiedHeader
Related codes
- Q92.0Whole chromosome trisomy, nonmosaicism (meiotic nondisjunction)Billable
- Q92.1Whole chromosome trisomy, mosaicism (mitotic nondisjunction)Billable
- Q92.2Partial trisomyBillable
- Q92.5Duplications with other complex rearrangementsBillable
- Q92.6Marker chromosomesHeader
- Q92.7Triploidy and polyploidyBillable
- Q92.9Trisomy and partial trisomy of autosomes, unspecifiedBillable