2026 ICD-10-CM Diagnosis Code M35.89Other specified systemic involvement of connective tissue
ICD-10-CM Codes›M00–M99›M30-M36›M35
- Billable — Valid for Submission
- CC — Complication or Comorbidity
- Chronic Condition
M35.89 is a billable ICD-10-CM diagnosis code for other specified systemic involvement of connective tissue. It is valid on HIPAA claims for fiscal year 2026 (October 1, 2025 through September 30, 2026) and groups to MS-DRG 545 through 547. 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 2 closely related codes. In AHRQ's Clinical Classifications Software (CCSR), this diagnosis falls under Systemic lupus erythematosus and connective tissue disorders.
M35.89 no longer risk-adjusts for Medicare Advantage: it mapped to HCC 40 under the retired CMS-HCC V24 model through payment year 2025 but maps to no category in the live V28 model. It still risk-adjusts in the PACE (CMS-HCC V22) category 40, ESRD (V21) category 40, ESRD (V24) category 40, and RxHCC Part D (V08) category 84 for payment year 2026.
Code Identity
Code Classification
Medicare Risk Adjustment (HCC)Billing
M35.89 no longer risk-adjusts for Medicare Advantage: it maps to no payment category in the live CMS-HCC V28 model, although it still risk-adjusts in the other CMS models shown below.
Source: CMS Payment Year 2026 risk adjustment mappings and model software. Weights are relative factors, not dollar amounts; a beneficiary's total RAF also includes demographics and interactions. Browse all CMS-HCC categories.
Approximate SynonymsGuidance
Alternate terms and clinical phrases that map to this code.
- Antisynthetase syndrome
- Anti-synthetase syndrome due to dermatomyositis
- Antisynthetase syndrome due to polymyositis
- Collagen deficiency syndrome
- Cranial cerebrospinal fluid leak
- EMILIN-1-related connective tissue disease
- Eosinophilia myalgia syndrome
- Eosinophilia-myalgia syndrome from tryptophan
- Leak of cranial cerebrospinal fluid due to collagen deficiency syndrome
- Marden Walker syndrome
- Muscle eosinophilia
- Polyneuropathy in collagen malignant disease
- Satoyoshi syndrome
Index to Diseases and InjuriesGuidance
Alphabetical index entries that point to this code.
Disease, diseased See Also: Syndrome;
Syndrome See Also: Disease;
eosinophilia-myalgia M35.89
Clinical ClassificationClinical
AHRQ’s CCSR groups this code into broader clinical categories.
Clinical InformationClinical
Autoimmune Hypophysitis|Lymphocytic Hypophysitis
an autoimmune condition affecting the pituitary gland, characterized by lymphocytic infiltration, commonly presenting with pituitary hormone deficiencies.Grade 1 Hypophysitis, CTCAE|Grade 1 Hypophysitis
asymptomatic or mild symptoms; clinical or diagnostic observations only; intervention not indicatedGrade 2 Hypophysitis, CTCAE|Grade 2 Hypophysitis
moderate; minimal, local or noninvasive intervention indicated; limiting age-appropriate instrumental adlGrade 3 Hypophysitis, CTCAE|Grade 3 Hypophysitis
severe or medically significant but not immediately life-threatening; hospitalization or prolongation of existing hospitalization indicated; limiting self care adlGrade 4 Hypophysitis, CTCAE|Grade 4 Hypophysitis
life-threatening consequences; urgent intervention indicatedGrade 5 Hypophysitis, CTCAE|Grade 5 Hypophysitis
deathHypophysitis
an inflammatory process in the pituitary gland.Hypophysitis, CTCAE|Hypophysitis
a disorder characterized by inflammation and cellular infiltration of the pituitary gland.Lymphocytic Neurohypophysitis
an autoimmune condition affecting the posterior pituitary gland, which is characterized by lymphocytic infiltration, and which often presents as diabetes insipidus.
Patient EducationClinical
Connective Tissue Disorders
Your connective tissue supports many different parts of your body, such as your skin, eyes, and heart. It is like a "cellular glue" that gives your body parts their shape and helps keep them strong. It also helps some of your tissues do their work. It is made of many kinds of proteins. Cartilage and fat are types of connective tissue.
Read the full article at MedlinePlus
Courtesy of MedlinePlus, a service of the U.S. National Library of Medicine.
Code History & ChangesHistory
Replacement M35.89 replaces the following previously assigned code(s):
- M35.8 - Other specified systemic involvement of connective tissue
Questions About M35.89Overview
What is the ICD-10 code for other specified systemic involvement of connective tissue?
The ICD-10-CM code for other specified systemic involvement of connective tissue is M35.89 (sometimes written as M3589). It is billable on HIPAA-covered claims from October 1, 2025 through September 30, 2026.
Is M35.89 (Other specified systemic involvement of connective tissue) a billable code?
Yes. This is a billable ICD-10-CM code, specific enough to report other specified systemic involvement of connective tissue on HIPAA-covered claims from October 1, 2025 through September 30, 2026.
What MS-DRG does M35.89 group to?
When other specified systemic involvement of connective tissue is the principal diagnosis on an inpatient stay, it groups to MS-DRG 545, 546, 547, with relative weights from 0.8362 to 2.4817 depending on complications. Higher weights mean higher Medicare reimbursement.
Is M35.89 a CC or MCC?
CMS lists M35.89 as a CC (complication or comorbidity) for FY 2026. 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 2 closely related codes in its exclusion list.
Does M35.89 risk-adjust for Medicare Advantage payment?
Not for Medicare Advantage. M35.89 mapped to HCC 40 in the retired CMS-HCC V24 model, which last determined payment in 2025, but it maps to no category in the live V28 model; see all codes that no longer risk-adjust. It still risk-adjusts in the PACE (CMS-HCC V22) category 40 (Rheumatoid Arthritis and Inflammatory Connective Tissue Disease), ESRD (V21) category 40 (Rheumatoid Arthritis and Inflammatory Connective Tissue Disease), ESRD (V24) category 40 (Rheumatoid Arthritis and Inflammatory Connective Tissue Disease), and RxHCC Part D (V08) category 84 (Systemic Lupus Erythematosus and Other Systemic Connective Tissue Disorders).