Q12.8 ICD-10-CM Code: Other congenital lens malformations
Billing Status: YES. This is a valid, specific, and billable ICD-10-CM reference.
Coding at a Glance
- Tabular directives
- 1 inclusion term · 7 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 v43, Appendix B.
- MS-DRG 124 — OTHER DISORDERS OF THE EYE WITH MCC OR THROMBOLYTIC AGENT (MDC 02)
- MS-DRG 125 — OTHER DISORDERS OF THE EYE WITHOUT MCC (MDC 02)
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 Q12.8 in the official ICD-10-CM tabular list, quoted as published.
Source: CMS/CDC — ICD-10-CM Tabular ListRelease: FY2026Effective: October 1, 2025
Notes without a marker are published on Q12.8 itself; “inherited from” names the category or block whose note applies here.
Inclusion Terms
Alternative terms the tabular list files under this code.
- Microphakia
Excludes2 — Not Included Here
Conditions not covered by this code, but which may be reported alongside it when both are present.
- cleft lip and cleft palate (Q35-Q37) Compare Q12.8 vs Q35 →
- congenital malformation of cervical spine (Q05.0, Q05.5, Q67.5, Q76.0-Q76.4) Compare Q12.8 vs Q05.0 →
- congenital malformation of larynx (Q31.-) Compare Q12.8 vs Q31 →
- congenital malformation of lip NEC (Q38.0) Compare Q12.8 vs Q38.0 →
- congenital malformation of nose (Q30.-) Compare Q12.8 vs Q30 →
- congenital malformation of parathyroid gland (Q89.2) Compare Q12.8 vs Q89.2 →
- congenital malformation of thyroid gland (Q89.2) Compare Q12.8 vs Q89.2 →
Source: inherited from Q10-Q18
Coder workflow for Q12.8
MedCoder structured workflow — derived from this code’s own official record
Before you code Q12.8
- “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 Q12.8; 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).
ReviewQ12.0, Q12.1, Q12.2, Q12.3, Q12.4
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 Q12.8(7 notes)
Coding workflow: The conditions named in this note are not included in Q12.8. When the record documents both, both may be reported; the note is a boundary, not a prohibition.
CompareQ05.0, Q05.5, Q67.5, Q31, Q38.0, Q30
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 (8)
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.
- Cyst (colloid) (mucous) (simple) (retention), lens, congenital
- Distortion (s) (congenital), lens
- Hypoplasia, hypoplastic, zonule (ciliary)
- Lenticonus (anterior) (posterior) (congenital)
- Lentiglobus (posterior) (congenital)
- Microlentia (congenital)
- Microphakia (congenital)
- Persistence, persistent (congenital), capsule (opaque)
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 Q12.8 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 1 Excludes1 note: H27 — Other disorders of lens (via Q12.-).
These codes’ tabular lists mark this diagnosis as mutually exclusive — not reported together unless the conditions are documented as unrelated.
MS-DRG Grouper Relationships (FY2026)
Potential MS-DRG participation — not a DRG assignment.
FY2026 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 2 MS-DRGs: DRG 124 (MDC 02), DRG 125 (MDC 02).
From the CMS MS-DRG Definitions Manual (Appendices B and C). Actual DRG assignment depends on the complete claim.
Clinical classification (AHRQ CCSR):MAL005 — Congenital malformations of eye, ear, face, neck (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 (Congenital malformations of eye, ear, face, neck).
Q10.7 — Congenital malformation of orbit, Q11.0 — Cystic eyeball, Q11.1 — Other anophthalmos, Q11.2 — Microphthalmos, Q11.3 — Macrophthalmos, Q12.0 — Congenital cataract, Q12.1 — Congenital displaced lens, Q12.2 — Coloboma of lens, Q12.3 — Congenital aphakia, Q12.4 — Spherophakia, Q12.9 — Congenital lens malformation, unspecified, Q13.0 — Coloboma of iris, Q13.1 — Absence of iris, Q13.2 — Other congenital malformations of iris, Q13.3 — Congenital corneal opacity, Q13.4 — Other congenital corneal malformations, Q13.5 — Blue sclera, Q13.81 — Rieger anomaly, Q13.89 — Other congenital malformations of anterior segment of eye, Q13.9 — Congenital malformation of anterior segment of eye, unspecified, +41 more
Same Index main term, other category
The ICD-10-CM Index to Diseases and Injuries files this code under the main terms “Persistence, persistent”, “Hypoplasia, hypoplastic”, “Distortion”, …; these codes share that main term but sit in a different category of the Tabular List.
Q04.0 — Congenital malformations of corpus callosum (corpus callosum), Q04.3 — Other reduction deformities of brain (cerebellum), Q04.6 — Congenital cerebral cysts (porencephalic), Q04.8 — Other specified congenital malformations of brain (gyri), Q04.9 — Congenital malformation of brain, unspecified (brain), Q06.1 — Hypoplasia and dysplasia of spinal cord (spinal), Q06.8 — Other specified congenital malformations of spinal cord (neuroenteric), Q07.8 — Other specified congenital malformations of nervous system (nerve), Q10.3 — Other congenital malformations of eyelid (eyelid), Q11.2 — Microphthalmos (eye), Q13.89 — Other congenital malformations of anterior segment of eye (pupillary membrane), Q14.0 — Congenital malformation of vitreous humor (hyaloid, artery), Q14.1 — Congenital malformation of retina (artery, retinal), Q14.8 — Other congenital malformations of posterior segment of eye (hyaloid, system), Q15.8 — Other specified congenital malformations of eye (eye), Q16.3 — Congenital malformation of ear ossicles (ossicles, ear), Q16.4 — Other congenital malformations of middle ear (ear, middle), Q16.5 — Congenital malformation of inner ear (ear, inner), Q16.9 — Congenital malformation of ear causing impairment of hearing, unspecified (auditory canal, causing impairment of hearing), Q17.2 — Microtia (ear), +325 more
Contextual Map
Every relationship of Q12.8 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 Q12.8 with this related code 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-fy2026
- Q10-Q18 — Congenital malformations of eye, ear, face and neck[Hierarchy]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
Referenced by Excludes1 notes
- H27 — Other disorders of lens[Excludes1](via Q12.-): “congenital lens malformations (Q12.-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
Clinical classification (CCSR)
- MAL005 — Congenital malformations of eye, ear, face, neck[CCSR]— AHRQ CCSR for ICD-10-CM Diagnoses (HCUP)
MS-DRG Grouper
- DRG 124 — OTHER DISORDERS OF THE EYE WITH MCC OR THROMBOLYTIC AGENT[MS-DRG]: “OTHER DISORDERS OF THE EYE WITH MCC OR THROMBOLYTIC AGENT (MDC 02)”— CMS MS-DRG Definitions Manual (Appendix B) · FY2026
- DRG 125 — OTHER DISORDERS OF THE EYE WITHOUT MCC[MS-DRG]: “OTHER DISORDERS OF THE EYE WITHOUT MCC (MDC 02)”— CMS MS-DRG Definitions Manual (Appendix B) · FY2026
MDC crossing
- MDC 02 — Diseases and Disorders of the Eye[MDC crossing]: “Diseases and Disorders of the Eye — 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. 1,200 same-MDC procedures group here; browse them on the MDC page.”— CMS MS-DRG Definitions Manual · FY2026
Index entries
- Cyst (colloid) (mucous) (simple) (retention), lens, congenital[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Distortion (s) (congenital), lens[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Hypoplasia, hypoplastic, zonule (ciliary)[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Lenticonus (anterior) (posterior) (congenital)[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Lentiglobus (posterior) (congenital)[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Microlentia (congenital)[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Microphakia (congenital)[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Persistence, persistent (congenital), capsule (opaque)[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
Nearest codes
- Q12 — Congenital lens malformations[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- Q12.0 — Congenital cataract[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- Q12.1 — Congenital displaced lens[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- Q12.2 — Coloboma of lens[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- Q12.3 — Congenital aphakia[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- Q12.4 — Spherophakia[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- Q12.9 — Congenital lens malformation, unspecified[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
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 FY2026 tabular list, index and tables, effective October 1, 2025 Release, file and checksum · Publisher’s page
- Claim edits Official source data
- CMS Definitions of Medicare Code Edits — v43.1 (April 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 — v43 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. "Q12.8 — Other congenital lens malformations." ICD-10-CM FY2026. https://medcoder.ai/icd10/code/q12.8-other-congenital-lens-malformations
Change history
- FY2016 — October 1, 2015In the code set at ICD-10-CM adoptionOther congenital lens malformations
No changes since FY2016 — additions, deletions, description changes and billable-status changes are tracked through FY2027 (effective October 1, 2026), 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 Q12.8 in its code family, with their registry titles.