2020 ICD-10-CM Diagnosis Code Q89.01

Asplenia (congenital)

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
  • Q89.01 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 Q89.01 became effective on October 1, 2019.
  • This is the American ICD-10-CM version of Q89.01 - other international versions of ICD-10 Q89.01 may differ.
The following code(s) above Q89.01 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 Q89.01:
  • 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
  • Q89.0
    ICD-10-CM Diagnosis Code Q89.0

    Congenital absence and malformations of spleen

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Type 1 Excludes
    • isomerism of atrial appendages (with asplenia or polysplenia) (Q20.6)
    Congenital absence and malformations of spleen
Approximate Synonyms
  • Asplenia
  • Bilateral right-sidedness sequence
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.
  • Q89.01 is considered exempt from POA reporting.
ICD-10-CM Q89.01 is grouped within Diagnostic Related Group(s) (MS-DRG v37.0):
  • 814 Reticuloendothelial and immunity disorders with mcc
  • 815 Reticuloendothelial and immunity disorders with cc
  • 816 Reticuloendothelial and immunity disorders without cc/mcc

Convert Q89.01 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
Code annotations containing back-references to Q89.01:
  • Type 1 Excludes: D73.0
    ICD-10-CM Diagnosis Code D73.0

    Hyposplenism

      2016 2017 2018 2019 2020 Billable/Specific Code
    Applicable To
    • Atrophy of spleen
    Type 1 Excludes
    • asplenia (congenital) (Q89.01)
    • postsurgical absence of spleen (Z90.81)

Diagnosis Index entries containing back-references to Q89.01:
  • Absence (of) (organ or part) (complete or partial)
  • Agenesis
    • spleen Q89.01
  • Anomaly, anomalous (congenital) (unspecified type) Q89.9
    ICD-10-CM Diagnosis Code Q89.9

    Congenital malformation, unspecified

      2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
    Applicable To
    • Congenital anomaly NOS
    • Congenital deformity NOS
    • spleen Q89.09
      ICD-10-CM Diagnosis Code Q89.09

      Congenital malformations of spleen

        2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
      Applicable To
      • Congenital splenomegaly
      • agenesis Q89.01
  • Aplasia - see also Agenesis
    • spleen Q89.01
  • Asplenia (congenital) Q89.01
  • Ivemark's syndrome Q89.01 (asplenia with congenital heart disease)
  • Syndrome - see also Disease
    • splenic
      • agenesis Q89.01
    • Ivemark's Q89.01

ICD-10-CM Codes Adjacent To Q89.01
Q87.418 Marfan's syndrome with other cardiovascular manifestations
Q87.42 …… with ocular manifestations
Q87.43 …… with skeletal manifestation
Q87.5 Other congenital malformation syndromes with other skeletal changes
Q87.8 Other specified congenital malformation syndromes, not elsewhere classified
Q87.81 Alport syndrome
Q87.82 Arterial tortuosity syndrome
Q87.89 Other specified congenital malformation syndromes, not elsewhere classified
Q89 Other congenital malformations, not elsewhere classified
Q89.0 Congenital absence and malformations of spleen
Q89.01 Asplenia (congenital)
Q89.09 Congenital malformations of spleen
Q89.1 Congenital malformations of adrenal gland
Q89.2 Congenital malformations of other endocrine glands
Q89.3 Situs inversus
Q89.4 Conjoined twins
Q89.7 Multiple congenital malformations, not elsewhere classified
Q89.8 Other specified congenital malformations
Q89.9 Congenital malformation, unspecified
Q90 Down syndrome
Q90.0 Trisomy 21, nonmosaicism (meiotic nondisjunction)

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