Diagnosis Code

Q85.83 VON HIPPEL-LINDAU SYNDROME


Code Information

Diagnosis Code: Q85.83

Short Description: Von Hippel-Lindau syndrome

Long Description: Von Hippel-Lindau syndrome

The code Q85.83 is VALID for claim submission

Code Classification:

  • Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
    • Other congenital malformations (Q80-Q89)
      • Phakomatoses, not elsewhere classified (Q85)
        • Q85.83 Von Hippel-Lindau syndrome

Code Version: 2022 ICD-10-CM


Synonyms

  • Von Hippel-Lindau syndrome

Diagnostic Related Group(s)

The code Q85.83 is grouped in the following Diagnostic Related Group(s) (MS-DRG v39.0)
  • Myeloproliferative Disorders Or Poorly Differentiated Neoplasms With Major O.r. Procedures With Mcc (826)
  • Myeloproliferative Disorders Or Poorly Differentiated Neoplasms With Major O.r. Procedures With Cc (827)
  • Myeloproliferative Disorders Or Poorly Differentiated Neoplasms With Major O.r. Procedures Without Cc/mcc (828)

References to Index of Diseases and Injuries

The code Q85.83 has the following ICD-10-CM references to the Index of Diseases and Injuries
  • Code Also:
    • manifestations

Similar Codes

ICD-10 Code ICD-10 Description
Q85 Phakomatoses, not elsewhere classified
Q85.0 Neurofibromatosis (nonmalignant)
Q85.00 Neurofibromatosis, unspecified
Q85.01 Neurofibromatosis, type 1
Q85.02 Neurofibromatosis, type 2
Q85.03 Schwannomatosis
Q85.09 Other neurofibromatosis
Q85.1 Tuberous sclerosis
Q85.8 Other phakomatoses, not elsewhere classified
Q85.81 PTEN hamartoma tumor syndrome
Q85.82 Other Cowden syndrome
Q85.89 Other phakomatoses, not elsewhere classified
Q85.9 Phakomatosis, unspecified


This page was last updated on: 10/1/2023