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ICD-10-CM Codes
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Q00-Q99
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Q80-Q89
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Q87-
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2023 ICD-10-CM Diagnosis Code Q87.11
2023 ICD-10-CM Diagnosis Code Q87.11
Prader-Willi syndrome
2020 - New Code 2021 2022 2023 Billable/Specific Code POA Exempt
- Q87.11 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
- The 2023 edition of ICD-10-CM Q87.11 became effective on October 1, 2022.
- This is the American ICD-10-CM version of Q87.11 - other international versions of ICD-10 Q87.11 may differ.
The following code(s) above
Q87.11 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
Q87.11:
- Q00-Q99
2023 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)
- Q87
ICD-10-CM Diagnosis Code Q87
Other specified congenital malformation syndromes affecting multiple systems
2016 2017 2018 2019 2020 2021 2022 2023 Non-Billable/Non-Specific Code
Use Additional- code(s) to identify all associated manifestations
- Q87.1
ICD-10-CM Diagnosis Code Q87.1
Congenital malformation syndromes predominantly associated with short stature
2016 2017 2018 2019 2020 - Converted to Parent Code 2021 2022 2023 Non-Billable/Non-Specific Code
Type 1 Excludes- Ellis-van Creveld syndrome (Q77.6)
- Smith-Lemli-Opitz syndrome (E78.72)
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.
- Q87.11 is considered exempt from POA reporting.
ICD-10-CM Q87.11 is grouped within Diagnostic Related Group(s) (MS-DRG v40.0):
- 564 Other musculoskeletal system and connective tissue diagnoses with mcc
- 565 Other musculoskeletal system and connective tissue diagnoses with cc
- 566 Other musculoskeletal system and connective tissue diagnoses without cc/mcc
Code History
- 2020 (effective 10/1/2019): New code
- 2021 (effective 10/1/2020): No change
- 2022 (effective 10/1/2021): No change
- 2023 (effective 10/1/2022): No change
Code annotations containing back-references to Q87.11:
ICD-10-CM Codes Adjacent To Q87.11
Q85.89 Other phakomatoses, not elsewhere classified
Q85.9 Phakomatosis, unspecified
Q86 Congenital malformation syndromes due to known exogenous causes, not elsewhere classified
Q86.0 Fetal alcohol syndrome (dysmorphic)
Q86.1 Fetal hydantoin syndrome
Q86.2 Dysmorphism due to warfarin
Q86.8 Other congenital malformation syndromes due to known exogenous causes
Q87 Other specified congenital malformation syndromes affecting multiple systems
Q87.0 Congenital malformation syndromes predominantly affecting facial appearance
Q87.1 Congenital malformation syndromes predominantly associated with short stature
Q87.11
Prader-Willi syndrome
Q87.19 Other congenital malformation syndromes predominantly associated with short stature
Q87.2 Congenital malformation syndromes predominantly involving limbs
Q87.3 Congenital malformation syndromes involving early overgrowth
Q87.41 Marfan's syndrome with cardiovascular manifestations
Q87.410 Marfan's syndrome with aortic dilation
Q87.418 Marfan's syndrome with other cardiovascular manifestations
Q87.42 …… with ocular manifestations
Q87.43 …… with skeletal manifestation
Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.
