2027 ICD-10-CM Diagnosis Code I67.850Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
ICD-10-CM Codes›I00–I99›I60-I69›I67
- Billable — Valid for Submission
- CC — Complication or Comorbidity
- Chronic Condition
I67.850 is a billable ICD-10-CM diagnosis code for cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. It is valid on HIPAA claims for fiscal year 2027 (October 1, 2026 through September 30, 2027) and groups to MS-DRG 70 through 72. As a secondary diagnosis, it counts as a complication or comorbidity (CC) and moves an inpatient stay to a higher severity level within its MS-DRG family. It does not count, however, when the principal diagnosis is one of 182 closely related codes. Coders also document this condition as cathepsin A-related arteriopathy, strokes, leukoencephalopathy. In AHRQ's Clinical Classifications Software (CCSR), this diagnosis falls under Other and ill-defined cerebrovascular disease.
Code Identity
Code Classification
Approximate SynonymsGuidance
Alternate terms and clinical phrases that map to this code.
- Cathepsin A-related arteriopathy, strokes, leukoencephalopathy
- Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
- Small vessel cerebrovascular disease
Instructional NotesGuidance
Instructions from the official ICD-10-CM Tabular List that apply to I67.850: its own notes plus those printed at I67, block I60-I69, and Chapter 9. A note printed at a category, block or chapter applies to every code under it.
Applicable To
Conditions this code is used for: synonyms of the title or, for "other specified" codes, the conditions assigned to it. The list is not exhaustive.
- CADASIL
Excludes1
Not coded here: the excluded code is never reported together with this one, unless the two conditions are unrelated.
- traumatic intracranial hemorrhage (S06.-)
Excludes2
Not included here: the excluded condition is not part of this code, but a patient may have both, so both codes may be reported.
- sequelae of the listed conditions (I69.8)
- certain conditions originating in the perinatal period (P04-P96)
- certain infectious and parasitic diseases (A00-B99)
- complications of pregnancy, childbirth and the puerperium (O00-O9A)
- congenital malformations, deformations, and chromosomal abnormalities (Q00-Q99)
- endocrine, nutritional and metabolic diseases (E00-E88)
- injury, poisoning and certain other consequences of external causes (S00-T88)
- neoplasms (C00-D49)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
- systemic connective tissue disorders (M30-M36)
- transient cerebral ischemic attacks and related syndromes (G45.-)
Code Also
A second code may be needed to fully describe the condition; the note gives no sequencing direction.
Source: CMS ICD-10-CM Tabular List. How to read instructional notes.
Index to Diseases and InjuriesGuidance
Alphabetical index entries that point to this code.
Clinical ClassificationClinical
AHRQ’s CCSR groups this code into broader clinical categories.
Clinical InformationClinical
CADASIL
a familial, cerebral arteriopathy mapped to chromosome 19q12, and characterized by the presence of granular deposits in small cerebral arteries producing ischemic stroke; pseudobulbar palsy; and multiple subcortical infarcts (cerebral infarction). cadasil is an acronym for cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. cadasil differs from binswanger disease by the presence of migraine with aura and usually by the lack of history of arterial hypertension. (from bradley et al, neurology in clinical practice, 2000, p1146)
Patient EducationClinical
Brain Diseases
Your brain is the control center of your body. It controls your thoughts, memory, speech, and movement. It regulates the function of many organs. It's part of your nervous system, which also includes your spinal cord and peripheral nerves. The nervous system sends signals between your brain and the rest of the body.
Read the full article at MedlinePlus
Courtesy of MedlinePlus, a service of the U.S. National Library of Medicine.
Code History & ChangesHistory
Replacement I67.850 replaces the following previously assigned code(s):
- I67.89 - Other cerebrovascular disease
Questions About I67.850Overview
Is I67.850 (Hereditary cerebrovascular diseases) a billable code?
Yes. This is a billable ICD-10-CM code, specific enough to report cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy on HIPAA-covered claims from October 1, 2026 through September 30, 2027.
What MS-DRG does I67.850 group to?
When cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy is the principal diagnosis on an inpatient stay, it groups to MS-DRG 72, 70, 71, with relative weights from 0.7344 to 1.6089 depending on complications. Higher weights mean higher Medicare reimbursement.
Is I67.850 a CC or MCC?
CMS lists I67.850 as a CC (complication or comorbidity) for FY 2027. Reported as a secondary diagnosis, it moves the inpatient stay to a higher-weighted DRG within its severity family. It does not count when the principal diagnosis is one of the 182 closely related codes in its exclusion list.
Can I67.850 be reported with a code from I63.2?
Not as a rule. The Excludes1 note at I67, which applies to I67.850, lists "Occlusion and stenosis of precerebral artery causing cerebral infarction (I63.2-)". An Excludes1 note means the excluded code is never reported together with this one; the only exception is when the two conditions are unrelated to each other (Official Guidelines, Section I.A.12.a).