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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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Q95-
Balanced rearrangements and structural markers, not elsewhere classified
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2018/2019 ICD-10-CM Diagnosis Code Q95.9
Balanced rearrangement and structural marker, unspecified
2016 2017 2018 2019 Billable/Specific Code POA Exempt
- Q95.9 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
- The 2018/2019 edition of ICD-10-CM Q95.9 became effective on October 1, 2018.
- This is the American ICD-10-CM version of Q95.9 - other international versions of ICD-10 Q95.9 may differ.
The following code(s) above
Q95.9 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
Q95.9:
- Q00-Q99
2019 ICD-10-CM Range Q00-Q99
Congenital malformations, deformations and chromosomal abnormalitiesNote- Codes from this chapter are not for use on maternal records
Type 2 Excludes- inborn errors of metabolism (E70-E88)
- Q90-Q99
2019 ICD-10-CM Range Q90-Q99
Chromosomal abnormalities, not elsewhere classifiedType 2 Excludes- mitochondrial metabolic disorders (E88.4-)
- Q95
ICD-10-CM Diagnosis Code Q95
Balanced rearrangements and structural markers, not elsewhere classified
2016 2017 2018 2019 Non-Billable/Non-Specific Code
Includes- Robertsonian and balanced reciprocal translocations and insertions
- Balanced rearrangement and structural marker
- Chromosome anomaly
Present On AdmissionPOA 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.
- Q95.9 is considered exempt from POA reporting.
ICD-10-CM Q95.9 is grouped within Diagnostic Related Group(s) (MS-DRG v36.0):
- 951 Other factors influencing health status
Convert Q95.9 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
ICD-10-CM Codes Adjacent To Q95.9
Q93.89 Other deletions from the autosomes
Q93.9 Deletion from autosomes, unspecified
Q95 Balanced rearrangements and structural markers, not elsewhere classified
Q95.0 Balanced translocation and insertion in normal individual
Q95.1 Chromosome inversion in normal individual
Q95.2 Balanced autosomal rearrangement in abnormal individual
Q95.3 Balanced sex/autosomal rearrangement in abnormal individual
Q95.5 Individual with autosomal fragile site
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
Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.
