AutoICD API

Q87.11

Billable

Prader-Willi syndrome

Prader-Willi syndrome

Status

Billable / Specific

Parent Code

Q87.1

Coding Notes

Excludes 1

Codes that cannot be used together with this code (mutual exclusion)

Excludes 2

Conditions not included here, but the patient may have both

Use Additional Code

Additional codes that should follow this code

  • code(s) to identify all associated manifestations
Related Codes(1)
Q87.19

Other congen malform synd predom assoc with short stature

Billable
Also Known As / Clinical Terms(67)

SNOMED CT

UMLS

Clinical Terms

  • Prader-Labhart-Willi syndrome
  • Prader Willi Syndrome
  • Labhart-Willi Syndrome
  • Willi-Prader syndrome
  • prader willi syndromes
  • prader willy syndrome
  • Syndrome, Labhart-Willi-Prader-Fanconi
  • Prader Labhart Willi Syndrome
  • Labhart Willi Prader Fanconi Syndrome
  • prader willis syndrome
  • Willi Prader Syndrome
  • prader syndrome willy
  • prader willies syndrome
  • Prader-Willi syndrome (disorder)
  • PWS
  • syndrome willi prader
  • prader syndrome willis
  • Labhart Willi Syndrome
  • Syndrome, Willi-Prader
  • syndrome prader-willi
  • Genetic syndromic childhood obesity
  • Syndrome, Prader-Labhart-Willi
  • Labhart-Willi-Prader-Fanconi Syndrome
  • Syndrome, Prader-Willi
  • prader syndrome willies
  • Syndrome, Labhart-Willi
  • prader syndrome willi
Frequently Asked Questions
What is the ICD-10 code for prader-willi syndrome?

The ICD-10-CM code for prader-willi syndrome is Q87.11. The full clinical description is "Prader-Willi syndrome". Q87.11 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code Q87.11 mean?

ICD-10-CM code Q87.11 represents “Prader-Willi syndrome”. It is classified under Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities and is a billable/specific code that can be used on a claim.

Is Q87.11 a billable code?

Yes, Q87.11 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is Q87.11 in?

Q87.11 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).

What codes cannot be used with Q87.11?

Q87.11 has Excludes1 notes indicating codes that cannot be used together with it, including: Ellis-van Creveld syndrome (Q77.6); Smith-Lemli-Opitz syndrome (E78.72).

Are additional codes required with Q87.11?

Yes, when using Q87.11, also report: code(s) to identify all associated manifestations.

What SNOMED CT codes does Q87.11 map to?

Q87.11 maps to 2 SNOMED CT concepts: 1359763002, 89392001. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for Q87.11?

Q87.11 is linked to 1 UMLS Concept Unique Identifier: C0032897. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does Q87.11 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like prader-willi syndrome affect a person's functioning: body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

What is the ICD-11 equivalent of Q87.11?

There is no direct ICD-11 mapping available for Q87.11 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.

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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.