Q85.83
BillableVon Hippel-Lindau syndrome
Von Hippel-Lindau syndrome
Status
Billable / Specific
Parent Code
Q85.8Coding 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
Code Also
A second code may be required; sequencing depends on circumstances
- manifestations
Related Codes(3)
Also Known As / Clinical Terms(118)
SNOMED CT
UMLS
- Angiomatoses, Familial Cerebello-RetinalC0019562
- Angiomatoses, Familial CerebelloretinalC0019562
- Angiomatosis RetinaeC0019562
- Angiomatosis retinaeC0019562
- Angiomatosis, Familial Cerebello-RetinalC0019562
- Angiomatosis, Familial CerebelloretinalC0019562
- Cerebello-Retinal Angiomatoses, FamilialC0019562
- Cerebello-Retinal Angiomatosis, FamilialC0019562
- Cerebelloretinal Angiomatoses, FamilialC0019562
- Cerebelloretinal Angiomatosis, FamilialC0019562
- Cerebelloretinal angiomatosis, familialC0019562
- Cerebroretinal AngiomatosisC0019562
- Cerebroretinal angiomatosisC0019562
- Familial Cerebello Retinal AngiomatosisC0019562
- Familial Cerebello-Retinal AngiomatosesC0019562
- Familial Cerebello-Retinal AngiomatosisC0019562
- Familial Cerebelloretinal AngiomatosesC0019562
- Familial Cerebelloretinal AngiomatosisC0019562
- Familial cerebello-retinal angiomatosisC0019562
- HIPPEL LINDAU DISC0019562
- Hippel Lindau DiseaseC0019562
- Hippel Lindau syndromeC0019562
- Hippel-Lindau DiseaseC0019562
- Hippel-Lindau diseaseC0019562
- LINDAU DISC0019562
- LINDAUS DISC0019562
- Lindau DiseaseC0019562
- Lindau' diseaseC0019562
- Lindau's DiseaseC0019562
- Lindau's DiseasesC0019562
- Lindau's diseaseC0019562
- Lindaus DiseaseC0019562
- VHLC0019562
- VHL (Von Hippel-Lindau) syndromeC0019562
- VHL SyndromeC0019562
- VHL SyndromesC0019562
- VHL syndromeC0019562
- VHLSC0019562
- VON HIPPEL LINDAU DISC0019562
- VON HIPPEL-LINDAU SYNDROMEC0019562
- Von Hippel Lindau SyndromeC0019562
- Von Hippel Lindau syndromeC0019562
- Von Hippel-Lindau DiseaseC0019562
- Von Hippel-Lindau SyndromeC0019562
- Von Hippel-Lindau Syndrome (VHL)C0019562
- Von Hippel-Lindau diseaseC0019562
- Von Hippel-Lindau syndromeC0019562
- Von Hippel-Lindau syndrome (disorder)C0019562
- disease hippel lindaus vonC0019562
- disease hippel-lindau vonC0019562
- hippel lindau diseaseC0019562
- hippel lindau syndromeC0019562
- hippel lindau syndrome vonC0019562
- hippel lindau von diseaseC0019562
- hippel lindaus syndrome vonC0019562
- hippel-lindau diseaseC0019562
- lindau diseaseC0019562
- lindau von hippel diseaseC0019562
- lindau's diseaseC0019562
- von Hippel Lindau DiseaseC0019562
- von Hippel Lindau SyndromeC0019562
- von Hippel-Lindau DiseaseC0019562
- von Hippel-Lindau SyndromeC0019562
- von hippel lindau diseaseC0019562
- von hippel lindau syndromeC0019562
- von hippel-lindau diseaseC0019562
- von hippel-lindau syndromeC0019562
- von-hippel lindau diseaseC0019562
Clinical Terms
- disease hippel-lindau von
- LINDAU DIS
- hippel-lindau disease
- von hippel lindau disease
- Lindau' disease
- VHL
- disease hippel lindaus von
- VHL syndrome
- Familial Cerebello-Retinal Angiomatosis
- Cerebello-Retinal Angiomatoses, Familial
- Angiomatosis Retinae
- Von Hippel-Lindau Syndrome (VHL)
- Familial Cerebello Retinal Angiomatosis
- Von Hippel Lindau syndrome
- LINDAUS DIS
- Von Hippel-Lindau disease
- Cerebroretinal angiomatosis
- Lindau's Disease
- Familial Cerebelloretinal Angiomatosis
- VHL Syndromes
- Cerebelloretinal angiomatosis, familial
- von-hippel lindau disease
- hippel lindau von disease
- Cerebello-Retinal Angiomatosis, Familial
- VHL (Von Hippel-Lindau) syndrome
- Familial Cerebelloretinal Angiomatoses
- lindau von hippel disease
- Hippel Lindau Disease
- Lindaus Disease
- Angiomatosis, Familial Cerebelloretinal
- Familial Cerebello-Retinal Angiomatoses
- VHLS
- Cerebelloretinal Angiomatoses, Familial
- lindau disease
- Hippel Lindau syndrome
- Angiomatoses, Familial Cerebello-Retinal
- Lindau's Diseases
- Von Hippel-Lindau syndrome (disorder)
- hippel lindau syndrome von
- HIPPEL LINDAU DIS
- VON HIPPEL LINDAU DIS
- Angiomatoses, Familial Cerebelloretinal
- Angiomatosis, Familial Cerebello-Retinal
- hippel lindaus syndrome von
Frequently Asked Questions
What is the ICD-10 code for von hippel-lindau syndrome?
The ICD-10-CM code for von hippel-lindau syndrome is Q85.83. The full clinical description is "Von Hippel-Lindau syndrome". Q85.83 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q85.83 mean?
ICD-10-CM code Q85.83 represents “Von Hippel-Lindau 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 Q85.83 a billable code?
Yes, Q85.83 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q85.83 in?
Q85.83 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What codes cannot be used with Q85.83?
Q85.83 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); Meckel-Gruber syndrome (Q61.9).
What SNOMED CT codes does Q85.83 map to?
Q85.83 maps to 1 SNOMED CT concept: 46659004. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q85.83?
Q85.83 is linked to 1 UMLS Concept Unique Identifier: C0019562. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does Q85.83 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like von hippel-lindau 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 Q85.83?
There is no direct ICD-11 mapping available for Q85.83 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.
Automate ICD-10 Coding With AI
Send clinical text to the AutoICD API and get back structured ICD-10 codes with confidence scores. Integrates into any EHR or billing system in minutes.
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.