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 Term

  • Trisomies due to dicentrics
  • Trisomies due to extra rings
  • Trisomies due to isochromosomes
  • Individual with marker heterochromatin

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

  
Non-Billable/Non-Specific Code

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