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ICD-10/Q87.89

Q87.89 ICD-10-CM Code: Other specified congenital malformation syndromes, not elsewhere classified

Billing Status: YES. This is a valid, specific, and billable ICD-10-CM reference.

Inpatient Payment Groups (MS-DRG)

MS-DRGs this diagnosis helps define, as principal or secondary, per the CMS ICD-10-CM/PCS MS-DRG Definitions Manual v43.0 (FY2026), Appendix B.

  • MS-DRG 564 — OTHER MUSCULOSKELETAL SYSTEM AND CONNECTIVE TISSUE DIAGNOSES WITH MCC (MDC 08)
  • MS-DRG 565 — OTHER MUSCULOSKELETAL SYSTEM AND CONNECTIVE TISSUE DIAGNOSES WITH CC (MDC 08)
  • MS-DRG 566 — OTHER MUSCULOSKELETAL SYSTEM AND CONNECTIVE TISSUE DIAGNOSES WITHOUT CC/MCC (MDC 08)

A diagnosis appearing in a group's logic does not by itself determine the DRG assigned to a stay; the grouper uses the full claim.

Official Registry Overview & Definition

Other specified congenital malformation syndromes, not elsewhere classified is a billable ICD-10-CM diagnosis code (Q87.89).

Official Tabular Instructional Notes

Sequencing, inclusion, and exclusion notes published for Q87.89 in the official ICD-10-CM tabular list.

Excludes1 — Not Coded Here

Conditions that can never be reported with this code; the two are mutually exclusive.

  • Zellweger syndrome (E71.510)

Use Additional Code

Supplementary codes the tabular list directs you to add.

  • Use additional code(s) to identify all associated manifestations

Nearest Codes in This Family

Official ICD-10-CM classifications closest to Q87.89 in its code family, with their registry titles.

  • Q87.8 — Other specified congenital malformation syndromes, not elsewhere classified
  • Q87.81 — Alport syndrome
  • Q87.82 — Arterial tortuosity syndrome
  • Q87.83 — Bardet-Biedl syndrome
  • Q87.84 — Laurence-Moon syndrome
  • Q87.85 — MED13L syndrome
  • Q87.86 — Kleefstra syndrome
  • Q87.87 — Hao-Fountain Syndrome
  • Q87.88 — CTNNB1 syndrome
  • Q87.A — Loeys-Dietz syndrome

View all codes in the Q87 family

Indexed Clinical Terms (15)

Clinical term phrases from the official ICD-10-CM Index to Diseases and Injuries that map to this code.

  • Birt-Hogg-Dube syndrome
  • Cantrell's syndrome
  • Cerebro-hepato-renal syndrome
  • Syndrome, basal cell nevus
  • Syndrome, Birt-Hogg-Dube syndrome
  • Syndrome, cardiofaciocutaneous
  • Syndrome, congenital, affecting multiple systems NEC
  • Syndrome, congenital, muscular hypertrophy-cerebral
  • Syndrome, Glass
  • Syndrome, Gorlin's
  • Syndrome, Oliver-McFarlane
  • Syndrome, popliteal, web
  • Syndrome, SATB2-associated
  • Syndrome, Snyder-Robinson
  • Web, webbed (congenital), popliteal syndrome