ICD-10/Q99.8

Q99.8 ICD 2026 Code: Other specified chromosome abnormalities

Q99.8 is the authoritative medical code for Other specified chromosome abnormalities. This classification is used in medical billing and clinical recording to specify the clinical criteria for other specified chromosome abnormalities (ICD-10-CM Q99.8), ensuring healthcare documentation aligns with 2026 federal coding standards.

Billing Status: NO. This is a clinician non-billable / parent hierarchy grouping in the ICD-10-CM system.

Official Registry Overview & Definition

Other specified chromosome abnormalities is a non-billable ICD-10-CM category code Q99.8. A more specific billable subcode must be selected for claims submission. Excludes2 (not included here): mitochondrial metabolic disorders E88.4-.

Official Tabular Instructional Notes

Sequencing, inclusion, and exclusion notes published for Q99.8 in the official ICD-10-CM tabular list.

Excludes2 — Not Included Here

Conditions not covered by this code, but which may be reported alongside it when both are present.

  • mitochondrial metabolic disorders E88.4-

Frequently Asked Questions (FAQ) & Clinical Guidance

Can Q99.8 be billed directly?

No. Q99.8 (Other specified chromosome abnormalities) is a non-billable ICD-10-CM category code. A more specific billable subcode must be selected based on clinical documentation.

Can Q99.8 be reported alongside related conditions?

Per official ICD-10-CM Excludes2 instructions, Q99.8 and the following are not considered part of each other and may both be reported when both conditions are present: mitochondrial metabolic disorders (E88.4-).

Nearest Codes in This Family

Official ICD-10-CM classifications closest to Q99.8 in its code family, with their registry titles.

  • Q99 — Other chromosome abnormalities, not elsewhere classified
  • Q99.0 — Chimera 46, XX/46, XY
  • Q99.1 — 46, XX true hermaphrodite
  • Q99.2 — Fragile X chromosome
  • Q99.81 — Usher syndrome
  • Q99.811 — Usher syndrome, type 1
  • Q99.812 — Usher syndrome, type 2
  • Q99.813 — Usher syndrome, type 3
  • Q99.818 — Other Usher syndrome
  • Q99.819 — Usher syndrome, unspecified

View all 12 codes in the Q99 family

Indexed Clinical Terms (6)

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

  • Abnormal, abnormality, abnormalities, chromosome, chromosomal, sex
  • Abnormal, abnormality, abnormalities, chromosome, chromosomal, specified NEC
  • Additional, chromosome (s)
  • Anomaly, anomalous (congenital) (unspecified type), chromosomes, chromosomal, specified NEC
  • Syndrome, due to abnormality, chromosomal, specified NEC
  • Translocation, chromosomes NEC