2026 ICD-10-CM Diagnosis Code Q77.8Other osteochondrodysplasia with defects of growth of tubular bones and spine

ICD-10-CM Codes›Q00-Q99›Q65-Q79›Q77

ICD-10-CM Q77.8
CMSSource: CMS FY 2026 ICD-10-CM dataset · Effective Oct 1, 2025 – Sep 30, 2026

Q77.8 is a billable ICD-10-CM diagnosis code for other osteochondrodysplasia with defects of growth of tubular bones and spine. It is valid on HIPAA claims for fiscal year 2026 (October 1, 2025 through September 30, 2026) 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
Q77.8
Billable Status
Yes — Valid for Submission
Code Describes
Other osteochondrodysplasia with defects of growth of tubular bones and spine
Short Description
Oth osteochndrdys w defct of growth of tublr bones and spine
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 CodeQ77.8Other osteochondrodysplasia with defects of growth of tubular bones and spine

Present on Admission (POA)Billing

Q77.8 is exempt from POA reporting on inpatient claims to general acute care hospitals. Review other POA exempt codes.

Approximate SynonymsGuidance

Alternate terms and clinical phrases that map to this code.

  • Achondrogenesis
  • Acromesomelic dysplasia syndrome
  • Acromicric dysplasia
  • Astley-Kendall dysplasia
  • Bent bone dysplasia group
  • Bilateral congenital dysplasia of upper limbs
  • Bilateral Madelung deformity
  • Body height below reference range
  • Brachydactylous dwarfism Mseleni type
  • Camptomelic dysplasia
  • Congenital dysplasia of left upper limb
  • Congenital dysplasia of radius
  • Congenital dysplasia of right upper limb
  • Langer mesomelic dysplasia syndrome
  • Leri-Weill dyschondrosteosis
  • Lethal chondrodysplasia with fragmented bone
  • Lethal retarded ossification syndromes
  • Longitudinal deficiency of foot
  • Longitudinal deficiency of lower limb
  • Madelung's deformity
  • Metatropic dysplasia
  • Overgrowth, metaphyseal undermodeling, spondylar dysplasia syndrome
  • Parastremmatic dwarfism
  • Reduction deformity of lower limb
  • Schneckenbecken dysplasia
  • Thin ribs, tubular bones, dysmorphism syndrome
  • Trident hand
  • Wolcott-Rallison dysplasia

Index to Diseases and InjuriesGuidance

Alphabetical index entries that point to this code.

External Cause of Injuries IndexGuidance

References for this code in the External Cause of Injuries Index.

    • Dwarfism
      • metatropic
    • Leri-Weill syndrome
    • Osteochondrodysplasia
      • with defects of growth of tubular bones and spine
        • specified NEC

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

  • Metatropic Dysplasia

    an autosomal dominant condition caused by mutation(s) in the trpv4 gene, encoding transient receptor potential cation channel subfamily v member 4. it is characterized by a variable phenotype, which may include short limbs, kyphoscoliosis, and other skeletal abnormalities.

  • Achondrogenesis

    a rare group of disorders characterized by defective development of bones and cartilage.

  • Type II Achondrogenesis|Achondrogenesis, Type II|Hypochondrogenesis|Langer-Saldino Achondrogenesis

    an autosomal dominant condition caused by mutation(s) in the col2a1 gene, encoding collagen alpha-1(ii) chain. it is the most severe of a spectrum of disorders caused by mutations in the col2a1 gene, characterized by short limbs, small chest and lungs, and abnormal ossification of the spine and pelvis. often, infants die at birth or shortly thereafter.

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 Q77.8 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 2017–2025No changes
FY 2026CurrentCurrent code set, no changesEffective October 1, 2025 through September 30, 2026.

Questions About Q77.8Overview

Is Q77.8 a billable code?

Yes. This is a billable ICD-10-CM code, specific enough to report other osteochondrodysplasia with defects of growth of tubular bones and spine on HIPAA-covered claims from October 1, 2025 through September 30, 2026.

What MS-DRG does Q77.8 group to?

When other osteochondrodysplasia with defects of growth of tubular bones and spine is the principal diagnosis on an inpatient stay, it groups to MS-DRG 564, 565, 566, with relative weights from 0.7493 to 1.5436 depending on complications. Higher weights mean higher Medicare reimbursement.

Is Q77.8 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 other osteochondrodysplasia with defects of growth of tubular bones and spine on inpatient claims.

What is the ICD-9 equivalent of Q77.8?

Under the General Equivalence Mappings, other osteochondrodysplasia with defects of growth of tubular bones and spine converts to ICD-9-CM 756.4 (chondrodystrophy). The mapping is approximate, so confirm the match fits the documentation.

Footnotes

[1] Chronic - a chronic condition code indicates a condition lasting 12 months or longer and its effect on the patient based on one or both of the following criteria:

  • The condition results in the need for ongoing intervention with medical products,treatment, services, and special equipment
  • The condition places limitations on self-care, independent living, and social interactions.