2027 ICD-10-CM Diagnosis Code M72.9Fibroblastic disorder, unspecified

ICD-10-CM Codes›M00–M99›M70-M79›M72

ICD-10-CM M72.9
CMSSource: CMS FY 2027 ICD-10-CM dataset · Effective Oct 1, 2026 – Sep 30, 2027

M72.9 is a billable ICD-10-CM diagnosis code for fibroblastic disorder, unspecified. It is valid on HIPAA claims for fiscal year 2027 (October 1, 2026 through September 30, 2027) and groups to MS-DRG 557 through 558. Coders also document this condition as abscess of abdominal wall. In AHRQ's Clinical Classifications Software (CCSR), this diagnosis falls under Other specified connective tissue disease.

Code Identity

ICD-10-CM Code
M72.9
Billable Status
Yes — Valid for Submission
Code Describes
Fibroblastic disorder, unspecified
Short Description
Fibroblastic disorder, unspecified
Same as the full description in the CMS dataset.
Parent Code
Fibroblastic disorders

Code Classification

ChapterM00–M99Diseases of the musculoskeletal system and connective tissue
SectionM70-M79Other soft tissue disorders
CategoryM72Fibroblastic disorders
This CodeM72.9Fibroblastic disorder, unspecified

Approximate SynonymsGuidance

Alternate terms and clinical phrases that map to this code.

  • Abscess of abdominal wall
  • Cranial fasciitis
  • Disorder of rectus sheath
  • Fasciitis
  • Fibromatosis
  • Musculoskeletal fibromatosis
  • Nodular fasciitis
  • Rectus sheath abscess
  • Superficial fibromatosis

Instructional NotesGuidance

Instructions from the official ICD-10-CM Tabular List that apply to M72.9: its own notes plus those printed at M72 and Chapter 13. 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.

  • Fasciitis NOS
  • Fibromatosis NOS

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.

From M72 Fibroblastic disorders applies to 9 codes
  • retroperitoneal fibromatosis (D48.3)
From Chapter 13 (M00-M99) Diseases of the musculoskeletal system and connective tissue applies to 6,687 codes
  • arthropathic psoriasis (L40.5-)
  • certain conditions originating in the perinatal period (P04-P96)
  • certain infectious and parasitic diseases (A00-B99)
  • compartment syndrome (traumatic) (T79.A-)
  • 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)

Notes

General instructions on how these codes are used.

From Chapter 13 (M00-M99) Diseases of the musculoskeletal system and connective tissue applies to 6,687 codes
  • Use an external cause code following the code for the musculoskeletal condition, if applicable, to identify the cause of the musculoskeletal condition

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.

CCSR MUS025
Other specified connective tissue disease
Default principal diagnosis: inpatient Yes · outpatient Yes

Clinical InformationClinical

  • Fasciitis

    inflammation of the fascia. there are three major types: 1, eosinophilic fasciitis, an inflammatory reaction with eosinophilia, producing hard thickened skin with an orange-peel configuration suggestive of scleroderma and considered by some a variant of scleroderma; 2, necrotizing fasciitis (fasciitis, necrotizing), a serious fulminating infection (usually by a beta hemolytic streptococcus) causing extensive necrosis of superficial fascia; 3, nodular/pseudosarcomatous /proliferative fasciitis, characterized by a rapid growth of fibroblasts with mononuclear inflammatory cells and proliferating capillaries in soft tissue, often the forearm; it is not malignant but is sometimes mistaken for fibrosarcoma.

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.

Convert M72.9 to ICD-9-CMHistory

The closest ICD-9-CM equivalents under the General Equivalence Mappings.

ICD-9-CM
728.79 Fibromatoses NEC
Approximate The match is approximate rather than exact.
ICD-9-CM
729.4 Fasciitis NOS
Approximate The match is approximate rather than exact.

Code HistoryHistory

FY 2016AddedAdded to the ICD-10-CM code setEffective October 1, 2015, the first year of ICD-10-CM.
FY 2017–2026No changes
FY 2027CurrentCurrent code set, no changesEffective October 1, 2026 through September 30, 2027.

Questions About M72.9Overview

What is the ICD-10 code for fibroblastic disorder, unspecified?

The ICD-10-CM code for fibroblastic disorder, unspecified is M72.9 (sometimes written as M729). It is billable on HIPAA-covered claims from October 1, 2026 through September 30, 2027.

Is M72.9 (Fibroblastic disorders) a billable code?

Yes. This is a billable ICD-10-CM code, specific enough to report fibroblastic disorder, unspecified on HIPAA-covered claims from October 1, 2026 through September 30, 2027.

What MS-DRG does M72.9 group to?

When fibroblastic disorder, unspecified is the principal diagnosis on an inpatient stay, it groups to MS-DRG 557, 558, with relative weights from 0.8873 to 1.4883 depending on complications. Higher weights mean higher Medicare reimbursement.

What is the ICD-9 equivalent of M72.9?

Under the General Equivalence Mappings, fibroblastic disorder, unspecified converts to ICD-9-CM 728.79 (fibromatoses NEC) and 729.4 (fasciitis NOS). The mapping is approximate, so confirm the match fits the documentation.