Diagnosis Code

Q85.89 OTHER PHAKOMATOSES, NOT ELSEWHERE CLASSIFIED


Code Information

Diagnosis Code: Q85.89

Short Description: Other phakomatoses, not elsewhere classified

Long Description: Other phakomatoses, not elsewhere classified

The code Q85.89 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)
        • Q85.89 Other phakomatoses, not elsewhere classified

Code Version: 2022 ICD-10-CM


Synonyms

  • Abnormality of canalization and retrogressive differentiation
  • Angiomatosis of meninges
  • Angiomatosis of meninges
  • Basal cell nevus with comedones
  • Centrofacial lentiginosis syndrome
  • Congenital erector pili hamartoma
  • Congenital leptomeningeal angiomatosis
  • Congenital rhabdomyomatous mesenchymal hamartoma
  • Diffuse smooth muscle hamartoma
  • Epidermal nevus syndrome
  • Generalized basaloid follicular hamartoma syndrome
  • Gingival enlargement due to Sturge-Weber syndrome
  • Hamartoma of intestine
  • Hamartoma of intestine
  • Hamartoma of muscle
  • Hamartoma of muscle
  • Hamartoma of muscle
  • Hamartoma of muscle
  • Hamartoma of pilosebaceous apparatus
  • Hamartoma of pilosebaceous apparatus
  • Hamartoma of pilosebaceous apparatus
  • Hamartoma of small intestine
  • Hemangioma of face
  • Hemangioma of intracranial structure
  • Hereditary cutaneous vascular syndrome
  • Hereditary neurocutaneous angiomata
  • Perlman syndrome
  • Peutz-Jeghers polyps of small bowel
  • Peutz-Jeghers syndrome
  • Phakomatosis cesioflammea
  • Phakomatosis cesiomarmorata
  • Phakomatosis pigmentokeratotica
  • Phakomatosis spilorosea
  • Polyp of small intestine
  • Port-wine stain with associated anomalies
  • Port-wine stain with associated anomalies
  • Port-wine stain with associated anomalies
  • Port-wine stain with oculocutaneous melanosis
  • Port-wine stain with oculocutaneous melanosis
  • Port-wine stain with oculocutaneous melanosis
  • Rhabdomyomatous mesenchymal hamartoma
  • SCALP syndrome
  • Sebaceous nevus
  • Spinal hamartoma
  • Sturge-Weber syndrome
  • Vascular neurocutaneous syndrome

Diagnostic Related Group(s)

The code Q85.89 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 Q85.89 has the following ICD-10-CM references to the Index of Diseases and Injuries
  • Inclusion Terms:
    • Peutz-Jeghers syndrome
    • Sturge-Weber(-Dimitri) syndrome

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
Q85.83 Von Hippel-Lindau syndrome
Q85.9 Phakomatosis, unspecified


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