Q85.1 ICD-10-CM Code: Tuberous sclerosis
Billing Status: YES. This is a valid, specific, and billable ICD-10-CM reference.
Coding at a Glance
- Tabular directives
- 2 inclusion terms · 2 Excludes1
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 091 — OTHER DISORDERS OF NERVOUS SYSTEM WITH MCC (MDC 01)
- MS-DRG 092 — OTHER DISORDERS OF NERVOUS SYSTEM WITH CC (MDC 01)
- MS-DRG 093 — OTHER DISORDERS OF NERVOUS SYSTEM WITHOUT CC/MCC (MDC 01)
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.
Risk Adjustment (CMS-HCC)
Payment categories this diagnosis maps to under CMS-HCC V28, payment year 2026.
- HCC 23 — Prostate, Breast, and Other Cancers and Tumors
Other models: CMS-HCC V22 HCC 12 · RxHCC V08 HCC 22
Risk scores depend on the enrollee's full accepted diagnosis set and segment; a category mapping alone does not determine payment.
Coding instructions
Official Tabular Instructional Notes: the inclusion, exclusion and sequencing notes published for Q85.1 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 Q85.1 itself; “inherited from” names the category or block whose note applies here.
Inclusion Terms
Alternative terms the tabular list files under this code.
- Bourneville's disease
- Epiloia
Excludes1 — Not Coded Here
Conditions generally not reported together with this code (Excludes1) -- an error unless the two conditions are documented as unrelated to each other (ICD-10-CM Official Guidelines, Section I.A.12.a).
- ataxia telangiectasia Louis-Bar
- familial dysautonomia Riley-Day
Coder workflow for Q85.1
MedCoder structured workflow — derived from this code’s own official record
Before you code Q85.1
- Check the Excludes1 note: if the documentation supports a condition named there, do not simply proceed with Q85.1. Excludes1 conditions are not reported together with this code unless the record shows they are unrelated (Guidelines I.A.12.a).
Choose the right path
- Does the documentation support a condition named in Q85.1’s Excludes1 note?
Yes → Do not simply proceed: review the excluded code. Both are reported only when the record shows the two conditions are unrelated.
No → Continue.
Consider Q85.1. Then confirm the code is valid for the date of service in the Verify section.
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).
Official instructions as workflow
Excludes1 — check before selecting Q85.1(2 notes)
Coding workflow: If the documentation supports a condition named in this note, do not simply proceed with Q85.1: the two are not reported together. The one exception is when the record shows the two conditions are unrelated to each other.
See the official tabular notes · Guidelines I.A.12.a
Coding decision scenarios
Pattern scenarios for this code’s structure — decision rules, not clinical cases
Documentation: Both the condition Q85.1 describes and a condition named in its Excludes1 note are documented for the same encounter.
Coding question: Can both codes be reported?
Path: Review the Excludes1 note and the excluded code, and look for a provider statement on whether the two conditions are related.
Reason: Excludes1 means the two are not coded together; the exception is when the record shows the conditions are unrelated to each other (Guidelines I.A.12.a).
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 (12)
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.
- Bourneville's disease
- Disease, diseased, Bourneville (-Brissaud) (tuberous sclerosis)
- Disease, diseased, Pringle's (tuberous sclerosis)
- Epiloia
- Neurospongioblastosis diffusa
- Nevus, multiplex
- Phakomatosis, Bourneville's
- Pringle's disease (tuberous sclerosis)
- Sclerosis, sclerotic, brain (generalized) (lobular), tuberous
- Sclerosis, sclerotic, tuberous (brain)
- Syndrome, Bourneville (-Pringle)
- Tuberous sclerosis (brain)
Verify Before Coding
- CC as a secondary diagnosis (FY2026). Can raise the stay's MS-DRG severity tier.
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
MS-DRG Grouper Relationships (FY2026)
Potential MS-DRG participation — not a DRG assignment.
FY2026 MS-DRG: CC — Complication or Comorbidity. Reported as a secondary diagnosis, this code raises the stay's MS-DRG severity tier — except when the principal diagnosis is one of 8 clinically related codes on its CMS exclusion list.
Named in the grouper logic of 3 MS-DRGs: DRG 091 (MDC 01), DRG 092 (MDC 01), DRG 093 (MDC 01).
From the CMS MS-DRG Definitions Manual (Appendices B and C). Actual DRG assignment depends on the complete claim.
Clinical classification (AHRQ CCSR):MAL010 — Other specified and unspecified congenital anomalies (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 process (MS-DRG)
Acts as CC — raises the severity of other admissions. CMS groups these diagnoses into one MS-DRG principal-diagnosis exclusion process — a CC/MCC on this list never raises severity when the principal diagnosis is also on it.
Q85.81 — PTEN hamartoma tumor syndrome, Q85.82 — Other Cowden syndrome, Q85.83 — Von Hippel-Lindau syndrome, Q85.89 — Other phakomatoses, not elsewhere classified, Q85.9 — Phakomatosis, unspecified, Q89.7 — Multiple congenital malformations, not elsewhere classified, Q89.9 — Congenital malformation, unspecified
Same CMS-HCC risk category (V28)
CMS maps these diagnoses to the same Hierarchical Condition Category (Prostate, Breast, and Other Cancers and Tumors) for risk-adjusted payment.
D43.8 — Neoplasm of uncertain behavior of other specified parts of central nervous system, D43.9 — Neoplasm of uncertain behavior of central nervous system, unspecified, D44.3 — Neoplasm of uncertain behavior of pituitary gland, D44.4 — Neoplasm of uncertain behavior of craniopharyngeal duct, D44.5 — Neoplasm of uncertain behavior of pineal gland, D44.6 — Neoplasm of uncertain behavior of carotid body, D44.7 — Neoplasm of uncertain behavior of aortic body and other paraganglia, D45 — Polycythemia vera, D47.3 — Essential (hemorrhagic) thrombocythemia, D49.6 — Neoplasm of unspecified behavior of brain, Q85.00 — Neurofibromatosis, unspecified, Q85.01 — Neurofibromatosis, type 1, Q85.02 — Neurofibromatosis, type 2, Q85.03 — Schwannomatosis, Q85.09 — Other neurofibromatosis, Q85.81 — PTEN hamartoma tumor syndrome, Q85.82 — Other Cowden syndrome, Q85.83 — Von Hippel-Lindau syndrome, Q85.89 — Other phakomatoses, not elsewhere classified, Q85.9 — Phakomatosis, unspecified, +213 more
Related risk categories
These categories interact through CMS's HCC hierarchy — one can suppress the other's risk-adjustment weight when both are present on a claim.
Cancer Metastatic to Lung, Liver, Brain, and Other Organs; Acute Myeloid Leukemia Except Promyelocytic, Cancer Metastatic to Bone, Other and Unspecified Metastatic Cancer; Acute Leukemia Except Myeloid, Myelodysplastic Syndromes, Multiple Myeloma, and Other Cancers, Lung and Other Severe Cancers, Lymphoma and Other Cancers, Bladder, Colorectal, and Other Cancers
Same clinical category (CCSR)
AHRQ's Clinical Classifications Software groups these diagnoses under the same clinical category (Other specified and unspecified congenital anomalies).
Q83.9 — Congenital malformation of breast, unspecified, Q84.0 — Congenital alopecia, Q84.1 — Congenital morphological disturbances of hair, not elsewhere classified, Q84.2 — Other congenital malformations of hair, Q84.3 — Anonychia, Q84.4 — Congenital leukonychia, Q84.5 — Enlarged and hypertrophic nails, Q84.6 — Other congenital malformations of nails, Q84.8 — Other specified congenital malformations of integument, Q84.9 — Congenital malformation of integument, unspecified, Q85.8 — Other phakomatoses, not elsewhere classified, Q85.81 — PTEN hamartoma tumor syndrome, Q85.82 — Other Cowden syndrome, Q85.83 — Von Hippel-Lindau syndrome, Q85.89 — Other phakomatoses, not elsewhere classified, Q85.9 — Phakomatosis, unspecified, Q86.0 — Fetal alcohol syndrome (dysmorphic), Q86.1 — Fetal hydantoin syndrome, Q86.2 — Dysmorphism due to warfarin, Q86.8 — Other congenital malformation syndromes due to known exogenous causes, +59 more
Same Index main term, other category
The ICD-10-CM Index to Diseases and Injuries files this code under the main terms “Nevus”, “Sclerosis, sclerotic”; these codes share that main term but sit in a different category of the Tabular List.
K74.1 — Hepatic sclerosis (liver), K74.2 — Hepatic fibrosis with hepatic sclerosis (liver, with fibrosis), K76.1 — Chronic passive congestion of liver (liver, cardiac), K86.89 — Other specified diseases of pancreas (pancreas), M34.0 — Progressive systemic sclerosis (progressive, systemic), M34.2 — Systemic sclerosis induced by drug and chemical (systemic, drug-induced), M34.81 — Systemic sclerosis with lung involvement (systemic, with, lung involvement), M34.82 — Systemic sclerosis with myopathy (systemic, with, myopathy), M34.83 — Systemic sclerosis with polyneuropathy (systemic, with, polyneuropathy), M34.89 — Other systemic sclerosis (systemic, specified NEC), M34.9 — Systemic sclerosis, unspecified (systemic), N05.1 — Unspecified nephritic syndrome with focal and segmental glomerular lesions (focal and segmental), N26.9 — Renal sclerosis, unspecified (renal), N48.6 — Induration penis plastica (penis), N50.89 — Other specified disorders of the male genital organs (funicular), N83.8 — Other noninflammatory disorders of ovary, fallopian tube and broad ligament (ovary), N85.5 — Inversion of uterus (endometrium), N90.89 — Other specified noninflammatory disorders of vulva and perineum (corpus cavernosum, female), Q38.6 — Other congenital malformations of mouth (mouth, white sponge), Q82.5 — Congenital non-neoplastic nevus (Unna's), +70 more
Contextual Map
Every relationship of Q85.1 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.
Hierarchy
- Q00-QA1 — Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (Q00-QA1) (Q00-QA1)[Hierarchy]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- Q80-Q89 — Other congenital malformations[Hierarchy]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
Clinical classification (CCSR)
- MAL010 — Other specified and unspecified congenital anomalies[CCSR]— AHRQ CCSR for ICD-10-CM Diagnoses (HCUP)
Risk adjustment (CMS-HCC)
- HCC 23 — Prostate, Breast, and Other Cancers and Tumors [CMS-HCC]— CMS-HCC V28 · 2026
MS-DRG Grouper
- CC — Complication or Comorbidity [MS-DRG severity]: “As a secondary diagnosis this code can raise the stay's MS-DRG severity tier (CC).”— CMS MS-DRG Definitions Manual (Appendix C) · FY2026
- DRG 091 — OTHER DISORDERS OF NERVOUS SYSTEM WITH MCC[MS-DRG]: “OTHER DISORDERS OF NERVOUS SYSTEM WITH MCC (MDC 01)”— CMS MS-DRG Definitions Manual (Appendix B) · FY2026
- DRG 092 — OTHER DISORDERS OF NERVOUS SYSTEM WITH CC[MS-DRG]: “OTHER DISORDERS OF NERVOUS SYSTEM WITH CC (MDC 01)”— CMS MS-DRG Definitions Manual (Appendix B) · FY2026
- DRG 093 — OTHER DISORDERS OF NERVOUS SYSTEM WITHOUT CC/MCC[MS-DRG]: “OTHER DISORDERS OF NERVOUS SYSTEM WITHOUT CC/MCC (MDC 01)”— CMS MS-DRG Definitions Manual (Appendix B) · FY2026
MDC crossing
- MDC 01 — Diseases and Disorders of the Nervous System[MDC crossing]: “Diseases and Disorders of the Nervous System — 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. 8,892 same-MDC procedures group here; browse them on the MDC page.”— CMS MS-DRG Definitions Manual · FY2026
Index entries (12)
- Bourneville's disease[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Disease, diseased, Bourneville (-Brissaud) (tuberous sclerosis)[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Disease, diseased, Pringle's (tuberous sclerosis)[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Epiloia[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Neurospongioblastosis diffusa[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Nevus, multiplex[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Phakomatosis, Bourneville's[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Pringle's disease (tuberous sclerosis)[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- and 4 more
Nearest codes (13)
- Q85 — Phakomatoses, not elsewhere classified[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- Q85.0 — Neurofibromatosis (nonmalignant)[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- Q85.00 — Neurofibromatosis, unspecified[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- Q85.01 — Neurofibromatosis, type 1[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- Q85.02 — Neurofibromatosis, type 2[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- Q85.03 — Schwannomatosis[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- Q85.09 — Other neurofibromatosis[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- Q85.8 — Other phakomatoses, not elsewhere classified[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- and 5 more
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
- Risk adjustment Official source data
- 2026 Mid-Year Final ICD-10 Mappings + Model Software (cms.gov/files/zip/2026-midyear-final-icd-10-mappings.zip, 2026-midyear-final-model-software.zip) — CMS-HCC V28, PY2026 mid-year final release 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. "Q85.1 — Tuberous sclerosis." ICD-10-CM FY2026. https://medcoder.ai/icd10/code/q85.1-tuberous-sclerosis
Change history
- FY2016 — October 1, 2015In the code set at ICD-10-CM adoptionTuberous sclerosis
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 Q85.1 in its code family, with their registry titles.
- Q85.00 — Neurofibromatosis, unspecified
- Q85.01 — Neurofibromatosis, type 1
- Q85.02 — Neurofibromatosis, type 2
- Q85.03 — Schwannomatosis
- Q85.09 — Other neurofibromatosis
- Q85.8 — Other phakomatoses, not elsewhere classified
- Q85.81 — PTEN hamartoma tumor syndrome
- Q85.82 — Other Cowden syndrome
- Q85.83 — Von Hippel-Lindau syndrome
- Q85.89 — Other phakomatoses, not elsewhere classified