Q93.82
BillableWilliams syndrome
Williams syndrome
Status
Billable / Specific
Parent Code
Q93.8Coding Notes
Excludes 2
Conditions not included here, but the patient may have both
Related Codes(3)
Also Known As / Clinical Terms(86)
SNOMED CT
UMLS
- Aortic Stenoses, Hypercalcemia-SupravalvarC0175702
- Aortic Stenosis, Hypercalcemia-SupravalvarC0175702
- Beuren SyndromeC0175702
- Beuren syndromeC0175702
- CHROMOSOME 7q11.23 DELETION SYNDROME, 1.5- TO 1.8-MBC0175702
- Chromosome 7q11.23 Deletion SyndromeC0175702
- Contiguous Gene Syndrome, WilliamsC0175702
- Deletion 7q11.23C0175702
- Elfin facies syndromeC0175702
- Elfin facies with hypercalcemiaC0175702
- Fanconi Schlesinger syndromeC0175702
- Hypercalcemia Supravalvar Aortic StenosisC0175702
- Hypercalcemia-Supravalvar Aortic StenosesC0175702
- Hypercalcemia-Supravalvar Aortic StenosisC0175702
- Hypercalcemia-supravalvar aortic stenosisC0175702
- Monosomy 7q11.23C0175702
- Stenoses, Hypercalcemia-Supravalvar AorticC0175702
- Stenosis, Hypercalcemia-Supravalvar AorticC0175702
- Supravalvar Aortic Stenosis SyndromeC0175702
- Syndrome, BeurenC0175702
- Syndrome, WilliamsC0175702
- Syndrome, Williams-BeurenC0175702
- WBSC0175702
- WILLIAMS SYNDROMEC0175702
- WILLIAMS-BEUREN SYNDROMEC0175702
- WMSC0175702
- William syndromeC0175702
- Williams Barratt syndromeC0175702
- Williams Beuren SyndromeC0175702
- Williams Beuren syndromeC0175702
- Williams Contiguous Gene SyndromeC0175702
- Williams SyndromeC0175702
- Williams syndromeC0175702
- Williams syndrome (disorder)C0175702
- Williams-Beuren SyndromeC0175702
- Williams-Beuren Syndrome (WBS)C0175702
- Williams-Beuren syndromeC0175702
- beuren syndrome williamsC0175702
- elfin facies syndromeC0175702
- syndrome william beurenC0175702
- syndrome williamsC0175702
- william syndromeC0175702
- williams beuren syndromeC0175702
- williams syndromeC0175702
- williams' syndromeC0175702
- williams-beuren syndromeC0175702
Clinical Terms
- William syndrome
- 7q partial monosomy
- Elfin facies with hypercalcemia
- Fanconi Schlesinger syndrome
- Williams Beuren syndrome
- WILLIAMS-BEUREN SYNDROME
- Hypercalcemia Supravalvar Aortic Stenosis
- syndrome william beuren
- Elfin facies syndrome
- Contiguous Gene Syndrome, Williams
- Supravalvar Aortic Stenosis Syndrome
- williams' syndrome
- Aortic Stenosis, Hypercalcemia-Supravalvar
- Syndrome, Williams
- syndrome williams
- Monosomy 7q11.23
- Williams syndrome (disorder)
- Williams Barratt syndrome
- Stenosis, Hypercalcemia-Supravalvar Aortic
- beuren syndrome williams
- Stenoses, Hypercalcemia-Supravalvar Aortic
- Syndrome, Williams-Beuren
- Hypercalcemia-Supravalvar Aortic Stenoses
- WBS
- Hypercalcemia-supravalvar aortic stenosis
- WMS
- Aortic Stenoses, Hypercalcemia-Supravalvar
- Williams Contiguous Gene Syndrome
- Deletion 7q11.23
- Syndrome, Beuren
- Beuren syndrome
- CHROMOSOME 7q11.23 DELETION SYNDROME, 1.5- TO 1.8-MB
- Williams-Beuren Syndrome (WBS)
- Chromosome 7q11.23 Deletion Syndrome
Frequently Asked Questions
What is the ICD-10 code for williams syndrome?
The ICD-10-CM code for williams syndrome is Q93.82. The full clinical description is "Williams syndrome". Q93.82 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q93.82 mean?
ICD-10-CM code Q93.82 represents “Williams 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 Q93.82 a billable code?
Yes, Q93.82 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q93.82 in?
Q93.82 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What SNOMED CT codes does Q93.82 map to?
Q93.82 maps to 2 SNOMED CT concepts: 81304006, 63247009. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q93.82?
Q93.82 is linked to 1 UMLS Concept Unique Identifier: C0175702. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does Q93.82 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like williams 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 Q93.82?
There is no direct ICD-11 mapping available for Q93.82 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.