Q85.1
BillableTuberous sclerosis
Tuberous sclerosis
Status
Billable / Specific
Parent Code
Q85Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Bourneville's disease
- Epiloia
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
- inborn errors of metabolism (E70-E88)
Also Known As / Clinical Terms
SNOMED CT
- Adenoma sebaceum syndrome7199000
- Bourneville's disease7199000
- Epiloia7199000
- TS - Tuberous sclerosis7199000
- Tuberous sclerosis7199000
- Tuberous sclerosis syndrome7199000
- Adenoma sebaceum36025004
- Angiokeratoma in tuberous sclerosis36025004
- Facial angiofibroma36025004
- Fibrous skin tumor of tuberous sclerosis36025004
- Fibrous skin tumour of tuberous sclerosis36025004
- Pringle tumor36025004
- Pringle tumour36025004
- Pulmonary tuberous sclerosis233718008
- Ash leaf spot, tuberous sclerosis254243001
- Periungual fibroma264561009
- Pulmonary lymphangioleiomyomatosis277844007
- Angiofibroma302857002
- Juvenile angiofibroma302857002
- Benign neoplasm of nail apparatus402635005
- Periungual fibroma in tuberous sclerosis403823001
- Lymphangioleiomyomatosis due to tuberous sclerosis syndrome707433009
- ADPKD - autosomal dominant polycystic kidney disease765330003
- Autosomal dominant polycystic kidney disease765330003
- Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis765331004
- Tuberous sclerosis, polycystic kidney disease contiguous gene syndrome765331004
- Macule of skin829994007
- Lymphangiomyomatosis of connective tissue145751000119104
UMLS
- Adenoma sebaceum syndromeC0041341
- BOURNEVILLE DISC0041341
- BOURNEVILLES DISC0041341
- Bourneville DiseaseC0041341
- Bourneville PhacomatosisC0041341
- Bourneville PhakomatosisC0041341
- Bourneville Pringle DiseaseC0041341
- Bourneville Pringle's DiseaseC0041341
- Bourneville SyndromeC0041341
- Bourneville diseaseC0041341
- Bourneville phakomatosisC0041341
- Bourneville's DiseaseC0041341
- Bourneville's SyndromeC0041341
- Bourneville's diseaseC0041341
- Bourneville-Pringle DiseaseC0041341
- Bourneville-Pringle's DiseaseC0041341
- Bourneville-Pringles DiseaseC0041341
- Brain sclerosisC0041341
- Cerebral SclerosesC0041341
- Cerebral SclerosisC0041341
- Cerebral sclerosisC0041341
- Disease, Bourneville-PringleC0041341
- Disease, Bourneville-Pringle'sC0041341
- EpiloiaC0041341
- EpiloyaC0041341
- Phacomatosis, BournevilleC0041341
- Phakomatosis, BournevilleC0041341
- Sclerosis TuberosaC0041341
- Sclerosis tuberosaC0041341
- Sclerosis, CerebralC0041341
- Sclerosis, TuberoseC0041341
- Sclerosis, TuberousC0041341
- Syndrome, BournevilleC0041341
- Syndrome, Bourneville'sC0041341
- TS - Tuberous sclerosisC0041341
- TSCC0041341
- TUBEROSE SCLEROSISC0041341
- TUBEROUS SCLEROSIS COMPLEXC0041341
- Tuberose SclerosisC0041341
- Tuberose sclerosisC0041341
- Tuberous SclerosisC0041341
- Tuberous Sclerosis ComplexC0041341
- Tuberous sclerosisC0041341
- Tuberous sclerosis complexC0041341
- Tuberous sclerosis syndromeC0041341
- Tuberous sclerosis syndrome (disorder)C0041341
- adenoma sebaceumC0041341
- bourneville diseaseC0041341
- brain sclerosisC0041341
- cerebral sclerosisC0041341
- epiloiaC0041341
- phacomatosisC0041341
- sclerosis brainC0041341
- sclerosis tuberosaC0041341
- sclerosis tuberousC0041341
- tuberosa sclerosisC0041341
- tuberose sclerosisC0041341
- tuberous sclerosisC0041341
- tuberous sclerosis syndromeC0041341
Frequently Asked Questions
What is the ICD-10 code for tuberous sclerosis?
The ICD-10-CM code for tuberous sclerosis is Q85.1. The full clinical description is "Tuberous sclerosis". Q85.1 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q85.1 mean?
ICD-10-CM code Q85.1 represents "Tuberous sclerosis". 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 Q85.1 a billable code?
Yes, Q85.1 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q85.1 in?
Q85.1 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What codes cannot be used with Q85.1?
Q85.1 has Excludes1 notes indicating codes that cannot be used together with it, including: ataxia telangiectasia [Louis-Bar] (G11.3); familial dysautonomia [Riley-Day] (G90.1).
What SNOMED CT codes does Q85.1 map to?
Q85.1 maps to 14 SNOMED CT concepts: 765330003, 36025004, 7199000, 302857002, 254243001, and 9 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q85.1?
Q85.1 is linked to 1 UMLS Concept Unique Identifier: C0041341. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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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.