ICD-10 Diagnosis Code M72.8

Other fibroblastic disorders

Diagnosis Code M72.8

ICD-10: M72.8
Short Description: Other fibroblastic disorders
Long Description: Other fibroblastic disorders
This is the 2017 version of the ICD-10-CM diagnosis code M72.8

Valid for Submission
The code M72.8 is valid for submission for HIPAA-covered transactions.

Code Classification
  • Diseases of the musculoskeletal system and connective tissue (M00–M99)
    • Other soft tissue disorders (M70-M79)
      • Fibroblastic disorders (M72)

Information for Medical Professionals

Diagnostic Related Groups
The diagnosis code M72.8 is grouped in the following Diagnostic Related Group(s) (MS-DRG V34.0)


Convert to ICD-9 Additional informationCallout TooltipGeneral Equivalence Map
The ICD-10 and ICD-9 GEMs are used to facilitate linking between the diagnosis codes in ICD-9-CM and the new ICD-10-CM code set. The GEMs are the raw material from which providers, health information vendors and payers can derive specific applied mappings to meet their needs.

  • Fibroblastic rheumatism
  • Hereditary camptodactyly
  • Infantile digital fibromatosis
  • Intravascular fasciitis
  • Ischemic fasciitis
  • Ossifying fasciitis
  • Pachydermodactyly
  • Proliferative fasciitis
  • Superficial fibromatosis
  • Superficial fibromatosis
  • Superficial fibromatosis

Index of Diseases and Injuries
References found for the code M72.8 in the Index of Diseases and Injuries:

Information for Patients

Connective Tissue Disorders

Connective tissue is the material inside your body that supports many of its parts. It is the "cellular glue" that gives your tissues their shape and helps keep them strong. It also helps some of your tissues do their work. Cartilage and fat are examples of connective tissue.

There are over 200 disorders that impact connective tissue. Some, like cellulitis, are the result of an infection. Injuries can cause connective tissue disorders, such as scars. Others, such as Ehlers-Danlos syndrome, Marfan syndrome, and osteogenesis imperfecta, are genetic. Still others, like scleroderma, have no known cause. Each disorder has its own symptoms and needs different treatment.

  • Dupuytrens contracture (Medical Encyclopedia)

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