October 1 update. Our PDGM and ICD-10 tools now use the FY2027 code set: 190 codes added, 30 deleted, and no existing code changed clinical group.

See what changed

ICD-10 · PDGM grouping

Q92 Other trisomies and partial trisomies of the autosomes, not elsewhere classified

All 9 codes in the Q92 family, with the PDGM clinical group, comorbidity subgroup and primary-position rule CMS assigns, read from the CMS grouper crosswalk v07.2.26 and the CDC FY2027 code file.

ICD-10-CM FY2027 · CMS grouper v07.2.26

Codes in family

9

Can lead a claim

8

Cannot lead a claim

1

What CMS assigns to Q92

8 of the 9 codes group to MMTA - Other; 1 is assigned no clinical group. None of the 9 is assigned a comorbidity subgroup. 8 of the 9 can lead a claim.

Every code in Q92

Descriptions are CDC’s FY2027 wording; where CMS’s grouper abbreviates one, its form is shown beneath.

CodeDescriptionPrimary positionClinical groupComorbidity subgroup
Q92.0Whole chromosome trisomy, nonmosaicism (meiotic nondisjunction)CMS: Whole chromosome trisomy, nonmosaic (meiotic nondisjunction)Can lead a claimANone
Q92.1Whole chromosome trisomy, mosaicism (mitotic nondisjunction)Can lead a claimANone
Q92.2Partial trisomyCan lead a claimANone
Q92.5Duplications with other complex rearrangementsCan lead a claimANone
Q92.6 Marker chromosomes
Q92.61Marker chromosomes in normal individualCan lead a claimANone
Q92.62Marker chromosomes in abnormal individualCan lead a claimANone
Q92.7Triploidy and polyploidyCan lead a claimANone
Q92.8Other specified trisomies and partial trisomies of autosomesCan lead a claimANone
Q92.9Trisomy and partial trisomy of autosomes, unspecifiedCannot lead a claimPrincipal diagnosis not assigned to a clinical groupNoneNone

Sources: CMS HH PPS Grouper Software v07.2.26, effective 2026-10-01, for the clinical group, comorbidity subgroup, code-first conventions and primary-position flags; CDC NCHS ICD-10-CM FY2027 code descriptions for the family title and code wording. This is the crosswalk Medicare runs a claim through. Grouping also depends on admission source, timing, the OASIS functional items and the rest of the diagnosis list.

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