Q85.83Billable
Von Hippel-Lindau syndrome
- Chapter
- 17. Congenital malformations, deformations and chromosomal abnormalities
- Category
- Q85
- Effective date
- October 1, 2026
Related codes in category Q85
Q85Phakomatoses, not elsewhere classifiedQ85.0Neurofibromatosis (nonmalignant)Q85.00Neurofibromatosis, unspecifiedYesQ85.01Neurofibromatosis, type 1YesQ85.02Neurofibromatosis, type 2YesQ85.03SchwannomatosisYesQ85.09Other neurofibromatosisYesQ85.1Tuberous sclerosisYesQ85.8Other phakomatoses, not elsewhere classifiedQ85.81PTEN hamartoma tumor syndromeYesQ85.82Other Cowden syndromeYesQ85.89Other phakomatoses, not elsewhere classifiedYes
Frequently asked questions
What is ICD-10 code Q85.83?
Q85.83 is an ICD-10-CM diagnosis code for Von Hippel-Lindau syndrome.
Is Q85.83 a billable code?
Yes. Q85.83 is billable and specific enough to be used on a claim.
What ICD-10-CM chapter is Q85.83 in?
Q85.83 falls under Chapter 17: Congenital malformations, deformations and chromosomal abnormalities.
When did Q85.83 become effective?
Q85.83 has been effective since October 1, 2026, per the CMS/CDC ICD-10-CM annual release.
What other codes are related to Q85.83?
Q85.83 belongs to category Q85, which includes 12 other codes — see the related codes list on this page.
ICD-10-CM data maintained by CDC/CMS (public domain). Always verify codes with authoritative sources before making coding or billing decisions.