2026 ICD-10-CM Diagnosis Code Q92.61Marker chromosomes in normal individual
ICD-10-CM Codes›Q00-Q99›Q90-Q99›Q92
- Billable — Valid for Submission
- POA Exempt
- Not Chronic
Q92.61 is a billable ICD-10-CM diagnosis code for marker chromosomes in normal individual. It is valid on HIPAA claims for fiscal year 2026 (October 1, 2025 through September 30, 2026). The code is exempt from POA reporting. Coders also document this condition as balanced rearrangement and structural marker. In AHRQ's Clinical Classifications Software (CCSR), this diagnosis falls under Chromosomal abnormalities.
Code Identity
Code Classification
Present on Admission (POA)Billing
Q92.61 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.
- Balanced rearrangement and structural marker
- Extra unidentified structurally abnormal chromosome
- Familial extra unidentified structurally abnormal chromosome
- Individual with marker heterochromatin
Index to Diseases and InjuriesGuidance
Alphabetical index entries that point to this code.
- Extra - See Also: Accessory;
- marker chromosomes (normal individual) - Q92.61
External Cause of Injuries IndexGuidance
References for this code in the External Cause of Injuries Index.
- Extra
- marker chromosomes (normal individual)
Clinical ClassificationClinical
AHRQ’s CCSR groups this code into broader clinical categories.
Patient EducationClinical
Genetic Disorders
Genetic disorders are health conditions caused by changes (also called mutations or variants) in your genes. Genes are parts of DNA found in your cells that carry instructions for how your body grows, develops, and functions. Many genes tell your body how to make proteins, which are needed for your body to work properly.
The full article covers:
- What are genetic disorders?
- What causes genetic disorders?
- What are the types of genetic disorders?
- What are the different ways a genetic disorder can be inherited?
- How are genetic disorders diagnosed?
Read the full article at MedlinePlus
Courtesy of MedlinePlus, a service of the U.S. National Library of Medicine.
Convert Q92.61 to ICD-9-CMHistory
The closest ICD-9-CM equivalents under the General Equivalence Mappings.
Code HistoryHistory
Questions About Q92.61Overview
Is Q92.61 (Marker chromosomes) a billable code?
Yes. This is a billable ICD-10-CM code, specific enough to report marker chromosomes in normal individual on HIPAA-covered claims from October 1, 2025 through September 30, 2026.
Is Q92.61 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 marker chromosomes in normal individual on inpatient claims.
What is the ICD-9 equivalent of Q92.61?
Under the General Equivalence Mappings, marker chromosomes in normal individual converts to ICD-9-CM 758.5 (autosomal anomalies NEC). The mapping is approximate, so confirm the match fits the documentation.
Footnotes
[1] Not chronic - A diagnosis code that does not fit the criteria for chronic condition (duration, ongoing medical treatment, and limitations) is considered not chronic. Some codes designated as not chronic are acute conditions. Other diagnosis codes that indicate a possible chronic condition, but for which the duration of the illness is not specified in the code description (i.e., we do not know the condition has lasted 12 months or longer) also are considered not chronic.
