2027 ICD-10-CM Diagnosis Code Q77.7Spondyloepiphyseal dysplasia

ICD-10-CM Codes›Q00-Q99›Q65-Q79›Q77

ICD-10-CM Q77.7
CMSSource: CMS FY 2027 ICD-10-CM dataset · Effective Oct 1, 2026 – Sep 30, 2027

Q77.7 is a billable ICD-10-CM diagnosis code for spondyloepiphyseal 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. In AHRQ's Clinical Classifications Software (CCSR), this diagnosis falls under Musculoskeletal congenital conditions.

Code Identity

ICD-10-CM Code
Q77.7
Billable Status
Yes — Valid for Submission
Code Describes
Spondyloepiphyseal dysplasia
Short Description
Spondyloepiphyseal dysplasia
Same as the full description in the CMS dataset.
Parent Code
Q77
Osteochondrodysplasia with defects of growth of tubular bones and spine

Code Classification

ChapterQ00-Q99Congenital malformations, deformations and chromosomal abnormalities
SectionQ65-Q79Congenital malformations and deformations of the musculoskeletal system
CategoryQ77Osteochondrodysplasia with defects of growth of tubular bones and spine
This CodeQ77.7Spondyloepiphyseal dysplasia

Present on Admission (POA)Billing

Q77.7 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.

  • Abnormally short fourth metatarsal
  • Brachymetatarsia
  • Brachymetatarsia of fourth metatarsal
  • Congenital conductive hearing loss
  • Congenital hypoplasia of bone of radius and/or ulna
  • Congenital hypoplasia of ulna
  • Congenital hypotrichia
  • Cono-spondylar dysplasia
  • Czech dysplasia metatarsal type
  • Degenerative polyarthritis
  • Dyggve-Melchior-Clausen syndrome
  • Eiken syndrome
  • EVEN-plus syndrome
  • Immuno-osseous dysplasia
  • Leber's amaurosis
  • Mild spondyloepiphyseal dysplasia due to COL2A1 mutation with early onset osteoarthritis
  • Mild spondyloepiphyseal dysplasia with premature onset arthrosis
  • MIR140-related spondyloepiphyseal dysplasia
  • Multiple epiphyseal dysplasia Al-Gazali type
  • Multiple epiphyseal dysplasia Beighton type
  • Oligodontia
  • Opsismodysplasia
  • Progressive conductive hearing loss
  • Progressive spondyloepimetaphyseal dysplasia, short stature, short fourth metatarsals, intellectual disability syndrome
  • Pseudoachondroplastic spondyloepiphyseal dysplasia syndrome
  • Roifman syndrome
  • Scoliosis in skeletal dysplasia
  • Sponastrime dysplasia
  • Spondyloepimetaphyseal disorder
  • Spondyloepimetaphyseal dysplasia aggrecan type
  • Spondyloepimetaphyseal dysplasia anauxetic type
  • Spondyloepimetaphyseal dysplasia Genevieve type
  • Spondyloepimetaphyseal dysplasia Handigodu type
  • Spondyloepimetaphyseal dysplasia Irapa type
  • Spondyloepimetaphyseal dysplasia Isidor type
  • Spondyloepimetaphyseal dysplasia matrilin-3 type
  • Spondyloepimetaphyseal dysplasia Missouri type
  • Spondyloepimetaphyseal dysplasia PAPSS2 type
  • Spondyloepimetaphyseal dysplasia Shohat type
  • Spondyloepimetaphyseal dysplasia with joint laxity Beighton type
  • Spondyloepimetaphyseal dysplasia with joint laxity, EXOC6B type
  • Spondyloepimetaphyseal dysplasia with multiple dislocations
  • Spondyloepimetaphyseal dysplasia, abnormal dentition syndrome
  • Spondyloepimetaphyseal dysplasia, hypotrichosis syndrome
  • Spondyloepimetaphyseal dysplasia, short limb, abnormal calcification syndrome
  • Spondyloepiphyseal dysplasia Cantu type
  • Spondyloepiphyseal dysplasia congenita
  • Spondyloepiphyseal dysplasia Kimberley type
  • Spondyloepiphyseal dysplasia MacDermot type
  • Spondyloepiphyseal dysplasia Maroteaux type
  • Spondyloepiphyseal dysplasia Reardon type
  • Spondyloepiphyseal dysplasia Stanescu type
  • Spondyloepiphyseal dysplasia tarda
  • Spondyloepiphyseal dysplasia tarda Kohn type
  • Spondyloepiphyseal dysplasia with congenital joint dislocations
  • Spondyloepiphyseal dysplasia with joint laxity
  • Spondyloepiphyseal dysplasia, craniosynostosis, cleft palate, cataract and intellectual disability syndrome
  • Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual disability, Leber congenital amaurosis syndrome
  • Spondylo-megaepiphyseal-metaphyseal dysplasia
  • Spondylometaphyseal dysplasia Golden type
  • Spondyloperipheral dysplasia
  • Spondyloperipheral dysplasia with short ulna syndrome
  • X-linked intellectual disability, cerebellar hypoplasia, spondyloepiphyseal dysplasia syndrome
  • X-linked spondyloepimetaphyseal dysplasia

Instructional NotesGuidance

Instructions from the official ICD-10-CM Tabular List that apply to Q77.7: its own notes plus those printed at Q77 and Chapter 17. A note printed at a category, block or chapter applies to every code under it.

Excludes1

Not coded here: the excluded code is never reported together with this one, unless the two conditions are unrelated.

From Q77 Osteochondrodysplasia with defects of growth of tubular bones and spine applies to 10 codes

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 Q77 Osteochondrodysplasia with defects of growth of tubular bones and spine applies to 10 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

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 Q77.7 to ICD-9-CMHistory

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

ICD-9-CM
756.4 Chondrodystrophy
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 Q77.7Overview

What is the ICD-10 code for spondyloepiphyseal dysplasia?

The ICD-10-CM code for spondyloepiphyseal dysplasia is Q77.7 (sometimes written as Q777). It is billable on HIPAA-covered claims from October 1, 2026 through September 30, 2027.

Is Q77.7 a billable code?

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

What MS-DRG does Q77.7 group to?

When spondyloepiphyseal 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 Q77.7 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 spondyloepiphyseal 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 Q77.7?

Under the General Equivalence Mappings, spondyloepiphyseal dysplasia converts to ICD-9-CM 756.4 (chondrodystrophy). The mapping is approximate, so confirm the match fits the documentation.