2027 ICD-10-CM Diagnosis Code Q77.3Chondrodysplasia punctata

ICD-10-CM Codes›Q00-Q99›Q65-Q79›Q77

ICD-10-CM Q77.3
CMSSource: CMS FY 2027 ICD-10-CM dataset · Effective Oct 1, 2026 – Sep 30, 2027

Q77.3 is a billable ICD-10-CM diagnosis code for chondrodysplasia punctata. 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
Q77.3
Billable Status
Yes — Valid for Submission
Code Describes
Chondrodysplasia punctata
Short Description
Chondrodysplasia punctata
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 CodeQ77.3Chondrodysplasia punctata

Present on Admission (POA)Billing

Q77.3 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.

  • Brachytelephalangic chondrodysplasia punctata
  • Chondrodysplasia punctata
  • Chondrodysplasia punctata due to maternal autoimmune disease
  • Chondrodysplasia punctata Toriello type
  • Chondrodysplasia punctata, Conradi-Hünermann type
  • Chondrodysplasia punctata, MT type
  • Chondrodysplasia punctata, X-linked dominant type
  • Chondrodysplasia punctata, X-linked recessive type
  • Disorder of cholesterol metabolism
  • Disorder of cholesterol synthesis
  • Greenberg dysplasia
  • Hyperphosphatasia-osteoectasia syndrome
  • Lethal chondrodysplasia with fragmented bone

Instructional NotesGuidance

Instructions from the official ICD-10-CM Tabular List that apply to Q77.3: 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.

On Q77.3 itself
  • Rhizomelic chondrodysplasia punctata (E71.540)
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

Clinical InformationClinical

  • Chondrodysplasia Punctata

    a heterogeneous group of bone dysplasias, the common character of which is stippling of the epiphyses in infancy. the group includes a severe autosomal recessive form (chondrodysplasia punctata, rhizomelic), an autosomal dominant form (conradi-hunermann syndrome), and a milder x-linked form. metabolic defects associated with impaired peroxisomes are present only in the rhizomelic form.

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 Q77.3 to ICD-9-CMHistory

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

ICD-9-CM
756.59 Osteodystrophy NEC
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 Q77.3Overview

What is the ICD-10 code for chondrodysplasia punctata?

The ICD-10-CM code for chondrodysplasia punctata is Q77.3 (sometimes written as Q773). It is billable on HIPAA-covered claims from October 1, 2026 through September 30, 2027.

Is Q77.3 a billable code?

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

What MS-DRG does Q77.3 group to?

When chondrodysplasia punctata 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 Q77.3 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 chondrodysplasia punctata on inpatient claims. The code appears in the Congenital malformations and deformations of the musculoskeletal system (Q65-Q79) range of the CMS exempt list.

Can Q77.3 be reported with E71.540?

Not as a rule. The Excludes1 note on Q77.3 lists "Rhizomelic chondrodysplasia punctata (E71.540)". An Excludes1 note means the excluded code is never reported together with this one; the only exception is when the two conditions are unrelated to each other (Official Guidelines, Section I.A.12.a).