2019 ICD-10-CM Diagnosis Code Q92.2

Partial trisomy

    2016 2017 2018 2019 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 2019 edition of ICD-10-CM Q92.2 became effective on October 1, 2018.
  • 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

      2016 2017 2018 2019 Billable/Specific Code POA Exempt
    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
    2019 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
    2019 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

      2016 2017 2018 2019 Non-Billable/Non-Specific Code
    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 v36.0):
  • 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

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

      2016 2017 2018 2019 Billable/Specific Code POA Exempt
    • chromosome specified NEC Q92.8
      ICD-10-CM Diagnosis Code Q92.8

      Other specified trisomies and partial trisomies of autosomes

        2016 2017 2018 2019 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

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.