Q95.8 ICD-10-CM Code: Other balanced rearrangements and structural markers
Billing Status: YES. This is a valid, specific, and billable ICD-10-CM reference.
Coding at a Glance
- Tabular directives
- 1 inclusion term · 1 Excludes2
Inpatient Payment Groups (MS-DRG)
Potential MS-DRG participation — not a DRG assignment.
MS-DRGs this diagnosis helps define, as principal or secondary, per the CMS ICD-10-CM/PCS MS-DRG Definitions Manual v44, Appendix B.
- MS-DRG 951 — OTHER FACTORS INFLUENCING HEALTH STATUS (MDC 23)
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.
Coding instructions
Official Tabular Instructional Notes: the inclusion, exclusion and sequencing notes published for Q95.8 in the official ICD-10-CM tabular list, quoted as published.
Source: CMS/CDC — ICD-10-CM Tabular ListRelease: FY2027Effective: October 1, 2026
Trace:FY2027 changesChange historyRelease, file and checksum
Notes without a marker are published on Q95.8 itself; “inherited from” names the category or block whose note applies here.
Includes
Conditions the official ICD-10-CM tabular list includes under this code.
- Robertsonian and balanced reciprocal translocations and insertions
Source: inherited from Q95
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-) Compare Q95.8 vs E88.4 →
Source: inherited from Q90-Q99
Coder workflow for Q95.8
MedCoder structured workflow — derived from this code’s own official record
Before you code Q95.8
- “Other” (NEC) means the condition is specified in the record but no dedicated code captures it. Confirm the documented form is not one a sibling code names before settling on Q95.8; if the record states no specifics at all, the unspecified sibling applies instead. “Other” codes are for documented conditions the classification gives no specific code; “unspecified” codes are for records lacking the detail (Guidelines I.A.9.a, I.A.9.b).
ReviewQ95.0, Q95.1, Q95.2, Q95.3, Q95.5
See the relationships section · Guide: Other vs unspecified (NEC vs NOS) →
Documentation check
- The provider’s diagnostic statement
- Codes are assigned from the provider’s documented diagnosis, not from clinical criteria, test values or a medication list (Guidelines I.A.19).
- Any detail beyond this code’s title
- What the record states that a more specific sibling code would capture — or its absence, which itself supports the unspecified code.
Official instructions as workflow
Excludes2 — not part of Q95.8(1 note)
Coding workflow: The conditions named in this note are not included in Q95.8. When the record documents both, both may be reported; the note is a boundary, not a prohibition.
CompareE88.4
See the official tabular notes · Guidelines I.A.12.b
Every row is derived from this code’s own record — its title, tabular notes, 7th-character family and same-category siblings — with fixed MedCoder wording; nothing is inferred about a patient. The official notes and guideline text are in the sections each row links to, and they control.
Code Overview
MedCoder summary Summary composed by MedCoder from this code's official ICD-10-CM record. The tabular instructional notes themselves appear verbatim below.
Indexed Clinical Terms (1)
Official source data — entries quoted as published, in the Index’s own lookup phrasing
Clinical term phrases from the official ICD-10-CM Index to Diseases and Injuries that map to this code. These are alphabetic-index entries shown as the Index writes them — lookup phrasing, not necessarily the wording of a final diagnosis.
Verify Before Coding
- No Medicare Code Editor or MS-DRG Definitions Manual restrictions apply to this code.
From the code registry, the Medicare Code Editor, and the MS-DRG Definitions Manual. Check it against a full claim in Claim Check.
Relationships & Classification
MedCoder structured relationships — computed from published CMS and AHRQ datasets
Other codes that name Q95.8 or its code family, from the CMS ICD-10-CM tabular instructional notes. Tabular-note edges are stored at the code family level that carries each note.
Referenced by 10 Excludes1 notes across 3 chapters: E25 — Adrenogenital disorders (via Q95.-), Q50 — Congenital malformations of ovaries, fallopian tubes and broad ligaments (via Q95.-), Q50-Q56 — Congenital malformations of genital organs (Q50-Q56) (via Q95.-), Q51 — Congenital malformations of uterus and cervix (via Q95.-), Q52 — Other congenital malformations of female genitalia (via Q95.-), Q53 — Undescended and ectopic testicle (via Q95.-), Q54 — Hypospadias (via Q95.-), Q55 — Other congenital malformations of male genital organs (via Q95.-), Q56 — Indeterminate sex and pseudohermaphroditism (via Q95.-), Z15 — Genetic susceptibility to disease (via Q95.-).
These codes’ tabular lists mark this diagnosis as mutually exclusive — not reported together unless the conditions are documented as unrelated.
Referenced by 1 Code First instruction: D84.81 — Immunodeficiency due to conditions classified elsewhere (via Q95.-).
Each of these codes carries a Code First note naming this condition — when that code is reported, THIS code is sequenced first, ahead of it.
MS-DRG Grouper Relationships (FY2027)
Potential MS-DRG participation — not a DRG assignment.
FY2027 MS-DRG: not on the CMS CC/MCC list — as a secondary diagnosis this code does not change MS-DRG severity for that release.
Named in the grouper logic of 1 MS-DRG: DRG 951 (MDC 23).
From the CMS MS-DRG Definitions Manual (Appendices B and C). Actual DRG assignment depends on the complete claim.
Clinical classification (AHRQ CCSR):MAL009 — Chromosomal abnormalities (default).
Clinical Classifications Software Refined (CCSR) for ICD-10-CM Diagnoses. Healthcare Cost and Utilization Project (HCUP), Agency for Healthcare Research and Quality.
Related Codes
Same clinical category (CCSR)
AHRQ's Clinical Classifications Software groups these diagnoses under the same clinical category (Chromosomal abnormalities).
Q93.81 — Velo-cardio-facial syndrome, Q93.82 — Williams syndrome, Q93.88 — Other microdeletions, Q93.89 — Other deletions from the autosomes, Q93.9 — Deletion from autosomes, unspecified, Q95.0 — Balanced translocation and insertion in normal individual, Q95.1 — Chromosome inversion in normal individual, Q95.2 — Balanced autosomal rearrangement in abnormal individual, Q95.3 — Balanced sex/autosomal rearrangement in abnormal individual, Q95.5 — Individual with autosomal fragile site, Q95.9 — Balanced rearrangement and structural marker, unspecified, Q96.0 — Karyotype 45, X, Q96.1 — Karyotype 46, X iso (Xq), Q96.2 — Karyotype 46, X with abnormal sex chromosome, except iso (Xq), Q96.3 — Mosaicism, 45, X/46, XX or XY, Q96.4 — Mosaicism, 45, X/other cell line(s) with abnormal sex chromosome, Q96.8 — Other variants of Turner's syndrome, Q96.9 — Turner's syndrome, unspecified, Q97.0 — Karyotype 47, XXX, Q97.1 — Female with more than three X chromosomes, +56 more
Contextual Map
Every relationship of Q95.8 in one view: hierarchy, official tabular instructions in both directions, clinical classification, risk adjustment, MS-DRG participation, index terms and change history — each edge carrying the CMS source it derives from.
Run Q95.8 with these 9 related codes in Claim Check
Hierarchy
- Q00-QA1 — Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (Q00-QA1) (Q00-QA1)[Hierarchy]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- Q90-Q99 — Chromosomal abnormalities, not elsewhere classified[Hierarchy]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
Referenced by Excludes1 notes (10)
- E25 — Adrenogenital disorders[Excludes1](via Q95.-): “chromosomal abnormalities (Q90-Q99)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
- Q50 — Congenital malformations of ovaries, fallopian tubes and broad ligaments[Excludes1](via Q95.-): “syndromes associated with anomalies in the number and form of chromosomes (Q90-Q99)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
- Q50-Q56 — Congenital malformations of genital organs (Q50-Q56)[Excludes1](via Q95.-): “syndromes associated with anomalies in the number and form of chromosomes (Q90-Q99)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
- Q51 — Congenital malformations of uterus and cervix[Excludes1](via Q95.-): “syndromes associated with anomalies in the number and form of chromosomes (Q90-Q99)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
- Q52 — Other congenital malformations of female genitalia[Excludes1](via Q95.-): “syndromes associated with anomalies in the number and form of chromosomes (Q90-Q99)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
- Q53 — Undescended and ectopic testicle[Excludes1](via Q95.-): “syndromes associated with anomalies in the number and form of chromosomes (Q90-Q99)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
- Q54 — Hypospadias[Excludes1](via Q95.-): “syndromes associated with anomalies in the number and form of chromosomes (Q90-Q99)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
- Q55 — Other congenital malformations of male genital organs[Excludes1](via Q95.-): “syndromes associated with anomalies in the number and form of chromosomes (Q90-Q99)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
- and 2 more
Referenced by Code First instructions
- D84.81 — Immunodeficiency due to conditions classified elsewhere[Code First](via Q95.-): “chromosomal abnormalities (Q90-Q99)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
Clinical classification (CCSR)
- MAL009 — Chromosomal abnormalities[CCSR]— AHRQ CCSR for ICD-10-CM Diagnoses (HCUP)
MS-DRG Grouper
- DRG 951 — OTHER FACTORS INFLUENCING HEALTH STATUS[MS-DRG]: “OTHER FACTORS INFLUENCING HEALTH STATUS (MDC 23)”— CMS MS-DRG Definitions Manual (Appendix B) · FY2027
MDC crossing
- MDC 23 — Factors Influencing Health Status and Other Contacts with Health Services[MDC crossing]: “Factors Influencing Health Status and Other Contacts with Health Services — the grouper's crossing between diagnoses and procedures: a principal diagnosis sets the MDC, and same-MDC procedures move the stay to its surgical DRGs. 1,258 same-MDC procedures group here; browse them on the MDC page.”— CMS MS-DRG Definitions Manual · FY2027
Index entries
- Rearrangement, chromosomal, balanced (in), specified NEC[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2027
Nearest codes
- Q95 — Balanced rearrangements and structural markers, not elsewhere classified[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- Q95.0 — Balanced translocation and insertion in normal individual[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- Q95.1 — Chromosome inversion in normal individual[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- Q95.2 — Balanced autosomal rearrangement in abnormal individual[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- Q95.3 — Balanced sex/autosomal rearrangement in abnormal individual[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- Q95.5 — Individual with autosomal fragile site[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- Q95.9 — Balanced rearrangement and structural marker, unspecified[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
Change history
- FY2016 — In the code set at ICD-10-CM adoption [Change history]— CMS release files (code change ledger) · icd10cm-fy2016
Sources for this page
Codes, titles, notes, index terms and mappings on this page are transcribed from the datasets below. Relationships MedCoder computed and text MedCoder wrote are labelled where they appear.
- Code, title, tabular notes and index terms Official source data
- CMS/CDC ICD-10-CM FY2027 tabular list, index and tables, effective October 1, 2026 Release, file and checksum · Publisher’s page
- Claim edits Official source data
- CMS Definitions of Medicare Code Edits — v44.0 (October 2026) Release, file and checksum · Publisher’s page
- Inpatient payment groups Official source data
- CMS MS-DRG Definitions Manual (incl. Appendix B diagnosis index, Appendix C CC/MCC list, Appendix E procedure index) and IPPS Final Rule tables — v44 Release, file and checksum · Publisher’s page
- Change history and date-of-service validity Official source data
- CMS ICD-10-CM release addenda, ingested release by release into the change ledger Release, file and checksum · Publisher’s page
- Comparisons, relationships and the contextual map MedCoder structured relationship
- Computed by MedCoder from the tabular notes and tables above; every derived relationship is marked as derived where it appears
- Summary and FAQ answers MedCoder explanation
- Written by MedCoder to explain the sources above: drafted with AI assistance, checked by a person against the release files, and labelled as MedCoder text where it appears. Not official text.
Labels on this page: Official source data · MedCoder structured relationship · MedCoder explanation. How to read the labels · All data sources and release dates
Cite this page
Reference this page in a research guide, syllabus or article. The release is included because code content changes each year.
MedCoder.ai. "Q95.8 — Other balanced rearrangements and structural markers." ICD-10-CM FY2027. https://medcoder.ai/icd10/code/q95.8-other-balanced-rearrangements-and-structural-markers
Change history
- FY2016 — October 1, 2015In the code set at ICD-10-CM adoptionOther balanced rearrangements and structural markers
No changes since FY2016 — additions, deletions, description changes and billable-status changes are tracked through FY2027, and none are recorded for this code. Note changes are tracked from FY2027 only.
Nearest Codes in This Family
Official ICD-10-CM classifications closest to Q95.8 in its code family, with their registry titles.
- Q95 — Balanced rearrangements and structural markers, not elsewhere classified
- Q95.0 — Balanced translocation and insertion in normal individual
- Q95.1 — Chromosome inversion in normal individual
- Q95.2 — Balanced autosomal rearrangement in abnormal individual
- Q95.3 — Balanced sex/autosomal rearrangement in abnormal individual
- Q95.5 — Individual with autosomal fragile site
- Q95.9 — Balanced rearrangement and structural marker, unspecified