Q80-Q89
Medium Complexity

Congenital malformations and deformations of the musculoskeletal system

Primary Specialty: Orthopedics
Last Updated: 2025-09-10

ICD-10 Codes (86)

83 billable
0 category headers
Q81
Billable
Epidermolysis bullosa
View
Q81.0
Billable
Epidermolysis bullosa simplex
View
Q81.1
Billable
Epidermolysis bullosa letalis
View
Q81.2
Billable
Epidermolysis bullosa dystrophica
View
Q81.8
Billable
Other epidermolysis bullosa
View
Q81.9
Billable
Epidermolysis bullosa, unspecified
View
Q82
Billable
Other congenital malformations of skin
View
Q82.0
Billable
Hereditary lymphedema
View
Q82.1
Billable
Xeroderma pigmentosum
View
Q82.2
Billable
Congenital cutaneous mastocytosis
View
Q82.3
Billable
Incontinentia pigmenti
View
Q82.4
Billable
Ectodermal dysplasia (anhidrotic)
View
Q82.5
Billable
Congenital non-neoplastic nevus
View
Q82.6
Billable
Congenital sacral dimple
View
Q82.8
Billable
Other specified congenital malformations of skin
View
Q82.9
Billable
Congenital malformation of skin, unspecified
View
Q83
Congenital malformations of breast
View
Q83.0
Billable
Congenital absence of breast with absent nipple
View
Q83.1
Billable
Accessory breast
View
Q83.2
Billable
Absent nipple
View
Q83.3
Billable
Accessory nipple
View
Q83.8
Billable
Other congenital malformations of breast
View
Q83.9
Billable
Congenital malformation of breast, unspecified
View
Q84
Other congenital malformations of integument
View
Q84.0
Billable
Congenital alopecia
View
Q84.1
Billable
Congenital morphological disturbances of hair, not elsewhere classified
View
Q84.2
Billable
Other congenital malformations of hair
View
Q84.3
Billable
Anonychia
View
Q84.4
Billable
Congenital leukonychia
View
Q84.5
Billable
Enlarged and hypertrophic nails
View
Q84.6
Billable
Other congenital malformations of nails
View
Q84.8
Billable
Other specified congenital malformations of integument
View
Q84.9
Billable
Congenital malformation of integument, unspecified
View
Q85
Billable
Phakomatoses, not elsewhere classified
View
Q85.0
Billable
Neurofibromatosis (nonmalignant)
View
Q85.00
Billable
Neurofibromatosis, unspecified
View
Q85.01
Billable
Neurofibromatosis, type 1
View
Q85.02
Billable
Neurofibromatosis, type 2
View
Q85.03
Billable
Schwannomatosis
View
Q85.09
Billable
Other neurofibromatosis
View
Q85.1
Billable
Tuberous sclerosis
View
Q85.8
Billable
Other phakomatoses, not elsewhere classified
View
Q85.81
Billable
PTEN hamartoma tumor syndrome
View
Q85.82
Billable
Other Cowden syndrome
View
Q85.83
Billable
Von Hippel-Lindau syndrome
View
Q85.89
Billable
Other phakomatoses, not elsewhere classified
View
Q85.9
Billable
Phakomatosis, unspecified
View
Q86
Billable
Congenital malformation syndromes due to known exogenous causes, not elsewhere classified
View
Q86.0
Billable
Fetal alcohol syndrome (dysmorphic)
View
Q86.1
Billable
Fetal hydantoin syndrome
View
Q86.2
Billable
Dysmorphism due to warfarin
View
Q86.8
Billable
Other congenital malformation syndromes due to known exogenous causes
View
Q87
Billable
Other specified congenital malformation syndromes affecting multiple systems
View
Q87.0
Billable
Congenital malformation syndromes predominantly affecting facial appearance
View
Q87.1
Billable
Congenital malformation syndromes predominantly associated with short stature
View
Q87.11
Billable
Prader-Willi syndrome
View
Q87.19
Billable
Other congenital malformation syndromes predominantly associated with short stature
View
Q87.2
Billable
Congenital malformation syndromes predominantly involving limbs
View
Q87.3
Billable
Congenital malformation syndromes involving early overgrowth
View
Q87.4
Billable
Marfan syndrome
View
Q87.40
Billable
Marfan syndrome, unspecified
View
Q87.41
Billable
Marfan syndrome with cardiovascular manifestations
View
Q87.410
Billable
Marfan syndrome with aortic dilation
View
Q87.418
Billable
Marfan syndrome with other cardiovascular manifestations
View
Q87.42
Billable
Marfan syndrome with ocular manifestations
View
Q87.43
Billable
Marfan syndrome with skeletal manifestation
View
Q87.5
Billable
Other congenital malformation syndromes with other skeletal changes
View
Q87.8
Billable
Other specified congenital malformation syndromes, not elsewhere classified
View
Q87.81
Billable
Alport syndrome
View
Q87.82
Billable
Arterial tortuosity syndrome
View
Q87.83
Billable
Bardet-Biedl syndrome
View
Q87.84
Billable
Laurence-Moon syndrome
View
Q87.85
Billable
MED13L syndrome
View
Q87.86
Billable
Kleefstra syndrome
View
Q87.89
Billable
Other specified congenital malformation syndromes, not elsewhere classified
View
Q89
Other congenital malformations, not elsewhere classified
View
Q89.0
Billable
Congenital absence and malformations of spleen
View
Q89.01
Billable
Asplenia (congenital)
View
Q89.09
Billable
Congenital malformations of spleen
View
Q89.1
Billable
Congenital malformations of adrenal gland
View
Q89.2
Billable
Congenital malformations of other endocrine glands
View
Q89.3
Billable
Situs inversus
View
Q89.4
Billable
Conjoined twins
View
Q89.7
Billable
Multiple congenital malformations, not elsewhere classified
View
Q89.8
Billable
Other specified congenital malformations
View
Q89.9
Billable
Congenital malformation, unspecified
View

Updates & Changes

FY 2026 Updates

Current Year

New Codes (1)

Q23.4
Hypoplastic left heart syndrome with mitral atresia

Revised Codes (1)

Q21.0
Ventricular septal defect - updated to include hemodynamic significance when known

Deleted Codes

No codes deleted in this range for FY 2026

Historical Changes

  • FY 2025: Routine maintenance updates with minor terminology clarifications
  • FY 2024: Enhanced specificity requirements for certain code ranges
  • FY 2023: Updated documentation guidelines for improved clarity

Upcoming Changes

  • Proposed updates pending review by Coordination and Maintenance Committee
  • Under consideration: Enhanced digital health integration codes

Implementation Guidance

  • Review all FY 2026 updates for Q80-Q89 codes before implementation
  • Always verify the most current codes in the ICD-10-CM manual
  • Ensure clinical documentation supports the selected diagnosis codes
  • +3 more guidance items...

Range Overview

high priority

The ICD-10 category Q80-Q89 encompasses congenital malformations and deformations of the musculoskeletal system. These codes are used to document conditions present at birth that affect the structure and function of the musculoskeletal system. The range includes a variety of conditions, from congenital deformities of the hip to congenital malformations of the spine and rib cage.

Key Usage Points:

  • These codes are used for conditions present at birth, not acquired conditions.
  • Each code specifies the particular malformation or deformation.
  • Some codes require additional codes to fully describe the condition.
  • These codes can be used across many medical specialties.
  • Documentation must clearly indicate the condition is congenital.

Coding Guidelines

When to Use:

  • When a patient presents with a congenital musculoskeletal condition.
  • When a congenital musculoskeletal condition is discovered during a routine examination.
  • When a congenital musculoskeletal condition is relevant to the patient's current medical treatment.
  • When a congenital musculoskeletal condition affects the patient's health status.

When NOT to Use:

  • When the condition is acquired, not congenital.
  • When the condition is not related to the musculoskeletal system.
  • When the condition is a normal variant, not a malformation or deformation.
  • When the condition is better described by another code.

Code Exclusions

Always check the latest ICD-10 guidelines for exclusions.

Documentation Requirements

Documentation for these codes must clearly indicate the condition is congenital and describe the specific malformation or deformation. It should also include any relevant clinical information, such as the impact on the patient's health status and any related conditions or complications.

Clinical Information:

  • Specific congenital malformation or deformation
  • Impact on patient's health status
  • Related conditions or complications
  • Relevant clinical findings

Supporting Evidence:

  • Medical history
  • Physical examination findings
  • Imaging studies
  • Surgical reports
Good Documentation Example:

Patient has a congenital malformation of the spine (scoliosis) impacting mobility. X-ray confirms diagnosis.

Poor Documentation Example:

Patient has back problems.

Common Documentation Errors:

  • Not specifying the condition is congenital
  • Not providing enough detail about the malformation or deformation
  • Not documenting related conditions or complications
  • Not including supporting evidence

Range Statistics

15
Total Codes
83
Billable
Complexity:
Medium
Primary Use:Clinical Documentation
Chapter:17

Coding Complexity

Medium
Complexity Rating

Coding for these conditions requires a good understanding of congenital musculoskeletal conditions and careful review of the medical documentation. It can be challenging to identify the specific malformation or deformation and to code related conditions or complications.

Key Factors:
  • Determining whether a condition is congenital
  • Identifying the specific malformation or deformation
  • Coding related conditions or complications
  • Navigating exclusions

Specialty Focus

These codes are used across many medical specialties, including orthopedics, pediatrics, and genetics. They are particularly important in specialties that treat congenital conditions or that need to account for these conditions in patient care.

Primary Specialties:
Orthopedics
40%
Pediatrics
30%
Genetics
20%
Clinical Scenarios:
  • Newborn diagnosed with clubfoot
  • Child with congenital scoliosis affecting mobility
  • Adult with known congenital hip dysplasia requiring surgery
  • Patient with genetic disorder associated with multiple congenital malformations

Resources & References

There are many resources available for coding congenital malformations and deformations of the musculoskeletal system, including the official ICD-10 guidelines, clinical reference books, and educational materials.

Official Guidelines:

  • ICD-10-CM Official Guidelines for Coding and Reporting
  • World Health Organization's ICD-10 Browser
  • National Center for Health Statistics ICD-10-CM Index

Clinical References:

  • Orthopedic textbooks
  • Pediatric textbooks
  • Genetics textbooks

Educational Materials:

  • Online coding courses
  • Coding webinars
  • Coding practice exercises

Frequently Asked Questions

Can I use these codes for acquired conditions?

No, these codes are specifically for congenital conditions. Acquired conditions should be coded with the appropriate codes from other categories.