Q92.6 - Marker chromosomes
- Applicable to Marker chromosomes
- The 2025 edition of ICD10-CM Q92.6 became effective on October 1, 2024.
- This is the American ICD10-CM version of Q92.6 - other international versions of ICD10 Q92.6 may differ.
- Q92.6 is a Non-Billable / Non-Specific ICD10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
- Q92.6 Code should not be used for billing or reimbursement purposes as there are multiple ICD-10 CM codes below it that contain a greater level of detail.
- Q92.6 - Marker chromosomes
- Q92.6 - Marker chromosomes
- Q92.61 - Marker chromosomes in normal individual
- Q92.62 - Marker chromosomes in abnormal individual
Inclusion terms help to clarify and specify the conditions or diseases covered by a particular ICD-10-CM code.
Inclusion Term:
- Trisomies due to dicentrics
- Trisomies due to extra rings
- Trisomies due to isochromosomes
- Individual with marker heterochromatin
Non-Billable/Non-Specific Code
The following codes above Q92.6 contain annotation back-references that may be applicable to Q92.6:
- Chapter: Q00-Q99 - Congenital malformations, deformations and chromosomal abnormalities
- Section: Q90-Q99 - Chromosomal abnormalities, not elsewhere classified
- Category: Q92 - Other trisomies and partial trisomies of the autosomes, not elsewhere classified
Browse other similar CM codes:
Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.
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