Specific code 2015 ICD-9-CM Diagnosis Code 756.54
Polyostotic fibrous dysplasia of bone
  • 2015
  • Billable Code
  • ICD-9-CM 756.54 will be replaced by an equivalent ICD-10-CM code (or codes) when the United States transitions from ICD-9-CM to ICD-10-CM on October 1, 2015.
  • ICD-9-CM 756.54 is a billable medical code that can be used to specify a diagnosis on a reimbursement claim.
Clinical Information
  • A genetic syndrome caused by mutations in the gnas1 gene. It is characterized by deformities and fractures of the bones, endocrine abnormalities including early puberty, and skin hyperpigmentation
  • Fibrous dysplasia of bone affecting several bones. When melanotic pigmentation (cafe-au-lait spots) and multiple endocrine hyperfunction are additionally associated it is referred to as albright syndrome
Convert to ICD-10-CM: 756.54 converts directly to:
  • 2015 ICD-10-CM Q78.1 Polyostotic fibrous dysplasia
ICD-9-CM Volume 2 Index entries containing back-references to 756.54:
  • Dysplasia - see also Anomaly
    • polyostotic fibrous 756.54
  • Polyostotic fibrous dysplasia 756.54
ICD-9-CM codes are used in medical billing and coding to describe diseases, injuries, symptoms and conditions. ICD-9-CM 756.54 is one of thousands of ICD-9-CM codes used in healthcare. Although ICD-9-CM and CPT codes are largely numeric, they differ in that CPT codes describe medical procedures and services. Can't find a code? Start at the root of ICD-9-CM, check the 2015 ICD-9-CM Index or use the search engine at the top of this page to lookup any code.