2021

  1. ICD-10-CM Codes
    2. ›
  2. Q00-Q99 Congenital malformations, deformations and chromosomal abnormalities
    3. ›
  3. Q90-Q99 Chromosomal abnormalities, not elsewhere classified
    4. ›
  4. Q97- Other sex chromosome abnormalities, female phenotype, not elsewhere classified
    5. ›
  5. 2021 ICD-10-CM Diagnosis Code Q97.8

2021 ICD-10-CM Diagnosis Code Q97.8

Other specified sex chromosome abnormalities, female phenotype

    2016 2017 2018 2019 2020 2021 Billable/Specific Code POA Exempt
  • Q97.8 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
  • Short description: Oth sex chromosome abnormalities, female phenotype
  • The 2021 edition of ICD-10-CM Q97.8 became effective on October 1, 2020.
  • This is the American ICD-10-CM version of Q97.8 - other international versions of ICD-10 Q97.8 may differ.
The following code(s) above Q97.8 contain annotation back-references
Annotation Back-References
In this context, annotation back-references refer to codes that contain:
  • Applicable To annotations, or
  • Code Also annotations, or
  • Code First annotations, or
  • Excludes1 annotations, or
  • Excludes2 annotations, or
  • Includes annotations, or
  • Note annotations, or
  • Use Additional annotations
that may be applicable to Q97.8:
  • Q00-Q99
    2021 ICD-10-CM Range Q00-Q99

    Congenital malformations, deformations and chromosomal abnormalities

    Note
    • Codes from this chapter are not for use on maternal records
    Type 2 Excludes
    • inborn errors of metabolism (E70-E88)
    Congenital malformations, deformations and chromosomal abnormalities
  • Q90-Q99
    2021 ICD-10-CM Range Q90-Q99

    Chromosomal abnormalities, not elsewhere classified

    Type 2 Excludes
    • mitochondrial metabolic disorders (E88.4-)
    Chromosomal abnormalities, not elsewhere classified
  • Q97
    ICD-10-CM Diagnosis Code Q97

    Other sex chromosome abnormalities, female phenotype, not elsewhere classified

      2016 2017 2018 2019 2020 2021 Non-Billable/Non-Specific Code
    Type 1 Excludes
    • Turner's syndrome (Q96.-)
    Other sex chromosome abnormalities, female phenotype, not elsewhere classified
Present On Admission
POA Help
"Present On Admission" is defined as present at the time the order for inpatient admission occurs — conditions that develop during an outpatient encounter, including emergency department, observation, or outpatient surgery, are considered POA.
  • Q97.8 is considered exempt from POA reporting.
ICD-10-CM Q97.8 is grouped within Diagnostic Related Group(s) (MS-DRG v38.0):
  • 742 Uterine and adnexa procedures for non-malignancy with cc/mcc
  • 743 Uterine and adnexa procedures for non-malignancy without cc/mcc
  • 760 Menstrual and other female reproductive system disorders with cc/mcc
  • 761 Menstrual and other female reproductive system disorders without cc/mcc

Convert Q97.8 to ICD-9-CM

Code History
  • 2016 (effective 10/1/2015): New code (first year of non-draft ICD-10-CM)
  • 2017 (effective 10/1/2016): No change
  • 2018 (effective 10/1/2017): No change
  • 2019 (effective 10/1/2018): No change
  • 2020 (effective 10/1/2019): No change
  • 2021 (effective 10/1/2020): No change

Diagnosis Index entries containing back-references to Q97.8:
  • Abnormal, abnormality, abnormalities - see also Anomaly
    • chromosome, chromosomal Q99.9
      ICD-10-CM Diagnosis Code Q99.9

      Chromosomal abnormality, unspecified

        2016 2017 2018 2019 2020 2021 Billable/Specific Code POA Exempt
      • sex Q99.8
        ICD-10-CM Diagnosis Code Q99.8

        Other specified chromosome abnormalities

          2016 2017 2018 2019 2020 2021 Billable/Specific Code POA Exempt
        • female phenotype Q97.9
          ICD-10-CM Diagnosis Code Q97.9

          Sex chromosome abnormality, female phenotype, unspecified

            2016 2017 2018 2019 2020 2021 Billable/Specific Code POA Exempt
          • specified NEC Q97.8
  • Absence (of) (organ or part) (complete or partial)
  • Accessory (congenital)
    • chromosome(s) NEC (nonsex) Q92.9
      ICD-10-CM Diagnosis Code Q92.9

      Trisomy and partial trisomy of autosomes, unspecified

        2016 2017 2018 2019 2020 2021 Billable/Specific Code POA Exempt
      • sex
        • female phenotype Q97.8
  • Anomaly, anomalous (congenital) (unspecified type) Q89.9
    ICD-10-CM Diagnosis Code Q89.9

    Congenital malformation, unspecified

      2016 2017 2018 2019 2020 2021 Billable/Specific Code POA Exempt
    Applicable To
    • Congenital anomaly NOS
    • Congenital deformity NOS
  • Mosaicism, mosaic (autosomal) (chromosomal)
  • Sex

ICD-10-CM Codes Adjacent To Q97.8
Q96.2 Karyotype 46, X with abnormal sex chromosome, except iso (Xq)
Q96.3 Mosaicism, 45, X/46, XX or XY
Q96.4 Mosaicism, 45, X/other cell line(s) with abnormal sex chromosome
Q96.8 Other variants of Turner's syndrome
Q96.9 Turner's syndrome, unspecified
Q97 Other sex chromosome abnormalities, female phenotype, not elsewhere classified
Q97.0 Karyotype 47, XXX
Q97.1 Female with more than three X chromosomes
Q97.2 Mosaicism, lines with various numbers of X chromosomes
Q97.3 Female with 46, XY karyotype
Q97.8 Other specified sex chromosome abnormalities, female phenotype
Q97.9 Sex chromosome abnormality, female phenotype, unspecified
Q98 Other sex chromosome abnormalities, male phenotype, not elsewhere classified
Q98.0 Klinefelter syndrome karyotype 47, XXY
Q98.1 Klinefelter syndrome, male with more than two X chromosomes
Q98.3 Other male with 46, XX karyotype
Q98.4 Klinefelter syndrome, unspecified
Q98.5 Karyotype 47, XYY
Q98.6 Male with structurally abnormal sex chromosome
Q98.7 Male with sex chromosome mosaicism
Q98.8 Other specified sex chromosome abnormalities, male phenotype

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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