2027 ICD-10-CM Diagnosis Code Q78.3Progressive diaphyseal dysplasia

ICD-10-CM Codes›Q00-Q99›Q65-Q79›Q78

ICD-10-CM Q78.3
CMSSource: CMS FY 2027 ICD-10-CM dataset · Effective Oct 1, 2026 – Sep 30, 2027

Q78.3 is a billable ICD-10-CM diagnosis code for progressive diaphyseal dysplasia. It is valid on HIPAA claims for fiscal year 2027 (October 1, 2026 through September 30, 2027) and groups to MS-DRG 564 through 566. The code is exempt from POA reporting. Coders also document this condition as craniodiaphyseal dysplasia. In AHRQ's Clinical Classifications Software (CCSR), this diagnosis falls under Musculoskeletal congenital conditions.

Code Identity

ICD-10-CM Code
Q78.3
Billable Status
Yes — Valid for Submission
Code Describes
Progressive diaphyseal dysplasia
Short Description
Progressive diaphyseal dysplasia
Same as the full description in the CMS dataset.
Parent Code
Q78
Other osteochondrodysplasias

Code Classification

ChapterQ00-Q99Congenital malformations, deformations and chromosomal abnormalities
SectionQ65-Q79Congenital malformations and deformations of the musculoskeletal system
CategoryQ78Other osteochondrodysplasias
This CodeQ78.3Progressive diaphyseal dysplasia

Present on Admission (POA)Billing

Q78.3 is exempt from POA reporting on inpatient claims to general acute care hospitals. Review the other POA exempt codes in Congenital malformations and deformations of the musculoskeletal system (Q65-Q79).

Approximate SynonymsGuidance

Alternate terms and clinical phrases that map to this code.

  • Craniodiaphyseal dysplasia
  • Diaphyseal dysplasia
  • Diaphyseal medullary stenosis with bone malignancy
  • Ghosal hematodiaphyseal dysplasia

Instructional NotesGuidance

Instructions from the official ICD-10-CM Tabular List that apply to Q78.3: its own notes plus those printed at Q78 and Chapter 17. 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.

  • Camurati-Engelmann syndrome

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 Q78 Other osteochondrodysplasias applies to 9 codes
  • congenital myotonic chondrodystrophy (G71.13)
From Chapter 17 (Q00-QA1) Congenital malformations, deformations and chromosomal abnormalities applies to 900 codes
  • inborn errors of metabolism (E70-E88)

Notes

General instructions on how these codes are used.

From Chapter 17 (Q00-QA1) Congenital malformations, deformations and chromosomal abnormalities applies to 900 codes
  • Codes from this chapter are not for use on maternal records

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 MAL008
Musculoskeletal congenital conditions
Default principal diagnosis: inpatient Yes · outpatient Yes

Clinical InformationClinical

  • Camurati-Engelmann Syndrome

    an autosomal dominant form of dysplasia that is characterized by progressive thickening of diaphyseal cortex of long bones. mutations in the gene that encodes transforming growth factor beta1 are one cause of this disorder.

Patient EducationClinical

Birth Defects

A birth defect is a problem that happens while a baby is developing in the mother's body. Most birth defects happen during the first 3 months of pregnancy. One out of every 33 babies in the United States is born with a birth defect.

The full article covers:

  • What are birth defects?
  • What causes birth defects?
  • Who is at risk of having a baby with birth defects?
  • How are birth defects diagnosed?
  • What are the treatments for birth defects?
  • Can birth defects be prevented?

Read the full article at MedlinePlus

Courtesy of MedlinePlus, a service of the U.S. National Library of Medicine.

Convert Q78.3 to ICD-9-CMHistory

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

ICD-9-CM
756.56 Mult epiphyseal dysplas
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 Q78.3Overview

What is the ICD-10 code for progressive diaphyseal dysplasia?

The ICD-10-CM code for progressive diaphyseal dysplasia is Q78.3 (sometimes written as Q783). It is billable on HIPAA-covered claims from October 1, 2026 through September 30, 2027.

Is Q78.3 (Other osteochondrodysplasias) a billable code?

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

What MS-DRG does Q78.3 group to?

When progressive diaphyseal dysplasia is the principal diagnosis on an inpatient stay, it groups to MS-DRG 564, 566, 565, with relative weights from 0.7374 to 1.4909 depending on complications. Higher weights mean higher Medicare reimbursement.

Is Q78.3 exempt from POA reporting?

Yes. CMS lists this code among those exempt from present on admission reporting, so hospitals do not assign a POA indicator for progressive diaphyseal dysplasia on inpatient claims. The code appears in the Congenital malformations and deformations of the musculoskeletal system (Q65-Q79) range of the CMS exempt list.

What is the ICD-9 equivalent of Q78.3?

Under the General Equivalence Mappings, progressive diaphyseal dysplasia converts to ICD-9-CM 756.56 (mult epiphyseal dysplas). The mapping is approximate, so confirm the match fits the documentation.