Q92.8 Other specified trisomies and partial trisomies of autosomes
Billable ICD-10-CM code, FY2026. Exempt from present-on-admission (POA) reporting.
Applicable to
- Duplications identified by fluorescence in situ hybridization (FISH)
- Duplications identified by in situ hybridization (ISH)
- Duplications seen only at prometaphase
Applies from Q92 Other trisomies and partial trisomies of the autosomes, not elsewhere classified
Includes
- unbalanced translocations and insertions
Excludes1 (never code together)
- trisomies of chromosomes 13, 18, 21 (Q90-Q91)
Risk adjustment (HCC)
- RxHCC V08: HCC 148 — Mild or Unspecified Intellectual Disability/Developmental Disorder
MS-DRG index
Defines the logic of DRG(s) 951 in MDC 23.
Approximate ICD-9-CM (GEMs)
758.5 Other conditions due to autosomal anomalies (approximate)
Code annotations containing back-references to Q92.8
Back-references to Q92
- Code First:
D84.81 Immunodeficiency due to conditions classified elsewhere ("chromosomal abnormalities (Q90-Q99)") - Type 1 Excludes:
E25 Adrenogenital disorders ("chromosomal abnormalities (Q90-Q99)") - Type 1 Excludes:
Z15 Genetic susceptibility to disease ("chromosomal anomalies (Q90-Q99)")
Diagnosis Index entries for Q92.8
- Accessory (congenital) › chromosome (s) NEC (nonsex) › 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 (q)(p)
- Syndrome › trisomy › 22
- Trisomy (syndrome) › chromosome specified NEC
- Trisomy (syndrome) › chromosome specified NEC › specified NEC
- Trisomy (syndrome) › specified NEC
- Trisomy (syndrome) › whole chromosome › specified NEC
- Trisomy (syndrome) › 20
- Trisomy (syndrome) › 22
Nearby codes
Q92.5 Duplications with other complex rearrangementsQ92.6 Marker chromosomesQ92.61 Marker chromosomes in normal individualQ92.62 Marker chromosomes in abnormal individualQ92.7 Triploidy and polyploidyQ92.8 Other specified trisomies and partial trisomies of autosomes (this code)Q92.9 Trisomy and partial trisomy of autosomes, unspecified