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ICD-10-CM Codes
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Q00-Q99
Congenital malformations, deformations and chromosomal abnormalities
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Q90-Q99
Chromosomal abnormalities, not elsewhere classified
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Q97-
Other sex chromosome abnormalities, female phenotype, not elsewhere classified
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2022 ICD-10-CM Diagnosis Code Q97
2022 ICD-10-CM Diagnosis Code Q97
Other sex chromosome abnormalities, female phenotype, not elsewhere classified
2016 2017 2018 2019 2020 2021 2022 Non-Billable/Non-Specific Code
- Q97 should not be used for reimbursement purposes as there are multiple codes below it that contain a greater level of detail.
- Short description: Oth sex chromosome abnormalities, female phenotype, NEC
- The 2022 edition of ICD-10-CM Q97 became effective on October 1, 2021.
- This is the American ICD-10-CM version of Q97 - other international versions of ICD-10 Q97 may differ.
Type 1 ExcludesType 1 Excludes Help
A type 1 excludes note is a pure excludes. It means "not coded here". A type 1 excludes note indicates that the code excluded should never be used at the same time as Q97. A type 1 excludes note is for used for when two conditions cannot occur together, such as a congenital form versus an acquired form of the same condition.
The following code(s) above
Q97 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:
- 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
- 2022 (effective 10/1/2021): No change
ICD-10-CM Codes Adjacent To Q97
Q95.8 Other balanced rearrangements and structural markers
Q95.9 Balanced rearrangement and structural marker, unspecified
Q96.1 Karyotype 46, X iso (Xq)
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
Q97.1 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
Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.
