ICD-10-CM Codes
Q00-Q99 Congenital malformations, deformations and chromosomal abnormalities
Q90-Q99 Chromosomal abnormalities, not elsewhere classified
Q92- Other trisomies and partial trisomies of the autosomes, not elsewhere classified
2020 ICD-10-CM Diagnosis Code Q92.2

2020 ICD-10-CM Diagnosis Code Q92.2

Partial trisomy

2016

2017

2018

2019

2020

Billable/Specific Code

POA Exempt

Q92.2 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
The 2020 edition of ICD-10-CM Q92.2 became effective on October 1, 2019.
This is the American ICD-10-CM version of Q92.2 - other international versions of ICD-10 Q92.2 may differ.

Applicable To

Less than whole arm duplicated
Whole arm or more duplicated

Type 1 Excludes

Type 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 Q92.2. 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.

partial trisomy due to unbalanced translocation (
ICD-10-CM Diagnosis Code Q92.5
Duplications with other complex rearrangements
Applicable To
- Partial trisomy due to unbalanced translocations
Code Also
- any associated deletions due to unbalanced translocations, inversions and insertions (Q93.7)
Q92.5
)

The following code(s) above Q92.2 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 Q92.2:

Q00-Q99
2020 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
2020 ICD-10-CM Range Q90-Q99
Chromosomal abnormalities, not elsewhere classified
Type 2 Excludes
- mitochondrial metabolic disorders (E88.4-)
Chromosomal abnormalities, not elsewhere classified
Q92
ICD-10-CM Diagnosis Code Q92
Other trisomies and partial trisomies of the autosomes, not elsewhere classified
Includes
- unbalanced translocations and insertions
Type 1 Excludes
- trisomies of chromosomes 13, 18, 21 (Q90-Q91)
Other trisomies and partial trisomies of the autosomes, not elsewhere classified

Approximate Synonyms

Partial trisomy syndromes

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.

Q92.2 is considered exempt from POA reporting.

ICD-10-CM Q92.2 is grouped within Diagnostic Related Group(s) (MS-DRG v37.0):

951 Other factors influencing health status

Convert Q92.2 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

Diagnosis Index entries containing back-references to Q92.2:

Trisomy (syndrome) Q92.9
ICD-10-CM Diagnosis Code Q92.9
Trisomy and partial trisomy of autosomes, unspecified
- chromosome specified NEC Q92.8
  ICD-10-CM Diagnosis Code Q92.8
  Other specified trisomies and partial trisomies of autosomes
  2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
  Applicable To
  Duplications identified by fluorescence in situ hybridization (FISH)
  Duplications identified by in situ hybridization (ISH)
  Duplications seen only at prometaphase
  - partial Q92.2

ICD-10-CM Codes Adjacent To Q92.2

Q91.1 Trisomy 18, mosaicism (mitotic nondisjunction)

Q91.2 Trisomy 18, translocation

Q91.3 Trisomy 18, unspecified

Q91.4 Trisomy 13, nonmosaicism (meiotic nondisjunction)

Q91.5 Trisomy 13, mosaicism (mitotic nondisjunction)

Q91.6 Trisomy 13, translocation

Q91.7 Trisomy 13, unspecified

Q92 Other trisomies and partial trisomies of the autosomes, not elsewhere classified

Q92.0 Whole chromosome trisomy, nonmosaicism (meiotic nondisjunction)

Q92.1 Whole chromosome trisomy, mosaicism (mitotic nondisjunction)

Q92.2 Partial trisomy

Q92.5 Duplications with other complex rearrangements

Q92.6 Marker chromosomes

Q92.61 …… in normal individual

Q92.62 …… in abnormal individual

Q92.7 Triploidy and polyploidy

Q92.8 Other specified trisomies and partial trisomies of autosomes

Q92.9 Trisomy and partial trisomy of autosomes, unspecified

Q93 Monosomies and deletions from the autosomes, not elsewhere classified

Q93.0 Whole chromosome monosomy, nonmosaicism (meiotic nondisjunction)

Q93.1 Whole chromosome monosomy, mosaicism (mitotic nondisjunction)

Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.

2020 ICD-10-CM Diagnosis Code Q92.2

Partial trisomy

Duplications with other complex rearrangements

Congenital malformations, deformations and chromosomal abnormalities

Chromosomal abnormalities, not elsewhere classified

Other trisomies and partial trisomies of the autosomes, not elsewhere classified

Trisomy and partial trisomy of autosomes, unspecified

Other specified trisomies and partial trisomies of autosomes