Q85.81 PTEN HAMARTOMA TUMOR SYNDROME

Code Information

Diagnosis Code: Q85.81

Short Description: PTEN hamartoma tumor syndrome

Long Description: PTEN hamartoma tumor syndrome

The code Q85.81 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)
    - Q85.81 PTEN hamartoma tumor syndrome

Code Version: 2022 ICD-10-CM

The code Q85.81 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)

The code Q85.81 has the following ICD-10-CM references to the Index of Diseases and Injuries

Inclusion Terms:
- PHTS
- PTEN related Cowden syndrome
Code Also:
- , if applicable, genetic susceptibility to malignant neoplasm (@Z15.0*-)

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
Q85.82	Other Cowden syndrome
Q85.83	Von Hippel-Lindau syndrome
Q85.89	Other phakomatoses, not elsewhere classified
Q85.9	Phakomatosis, unspecified

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