Diagnosis Code

Q15.8 OTHER SPECIFIED CONGENITAL MALFORMATIONS OF EYE


Code Information

Diagnosis Code: Q15.8

Short Description: Other specified congenital malformations of eye

Long Description: Other specified congenital malformations of eye

The code Q15.8 is VALID for claim submission

Code Classification:

  • Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
    • Congenital malformations of eye, ear, face and neck (Q10-Q18)
      • Other congenital malformations of eye (Q15)
        • Q15.8 Other specified congenital malformations of eye

Code Version: 2022 ICD-10-CM


Synonyms

  • Accessory breast
  • Accessory nipple
  • Accessory tragus
  • Anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome
  • Atrophia bulborum hereditaria
  • Atypical Norrie disease due to monosomy Xp11.3
  • Bilateral congenital anomaly of corneas
  • Bilateral congenital ocular melanocytosis of eyes
  • Choristoma of eye proper
  • Choristoma of eye proper
  • Choristoma of left eye proper
  • Choristoma of right eye proper
  • Congenital abnormality of nipple
  • Congenital epibulbar choristoma of bilateral eyes
  • Congenital exophthalmos
  • Congenital failure of eye elevation
  • Congenital fibrosis of inferior rectus muscle
  • Congenital fibrosis syndrome
  • Congenital malposition of eye
  • Congenital ocular melanocytosis of left eye
  • Congenital ocular melanocytosis of right eye
  • Congenital vascular anomaly of eye
  • Developmental malformation of branchial arch
  • Epibulbar lipodermoid, preauricular appendage, polythelia syndrome
  • Extraocular muscle restriction
  • Glaucoma due to chamber angle anomaly
  • Glaucoma due to chamber angle anomaly
  • Glaucoma of bilateral eyes due to chamber angle anomaly
  • Glaucoma of left eye due to chamber angle anomaly
  • Glaucoma of right eye due to chamber angle anomaly
  • Hamartoma of retina
  • Hamartoma of retina of right eye
  • Horizontal orbital dystopia
  • Hypoplasia of eye muscle
  • Hypoplasia of muscle
  • Isolated congenital megalocornea
  • Megalocornea
  • Megalocornea
  • Megalocornea
  • Megalocornea of bilateral eyes
  • Megalocornea with intellectual disability syndrome
  • Melanin pigmentation of eye
  • Melanin pigmentation of eye
  • Melanin pigmentation of eye
  • Melanin pigmentation of eye
  • Ocular melanosis
  • Orbital dystopia
  • Polyotia
  • Port-wine stain with associated anomalies
  • Port-wine stain with oculocutaneous melanosis
  • Rotational orbital dystopia
  • Spondylo-ocular syndrome
  • Vertical orbital dystopia

Diagnostic Related Group(s)

The code Q15.8 is grouped in the following Diagnostic Related Group(s) (MS-DRG v39.0)
  • Other Disorders Of The Eye With Mcc Or Thrombolytic Agent (124)
  • Other Disorders Of The Eye Without Mcc (125)

Crosswalk Information

ICD-10 Code ICD-9 Code ICD-9 Description
Q15.8 Right Arrow 743.8 Eye anomalies NEC

This ICD-10 to ICD-9 data is based on the 2018 General Equivalency Mapping (GEM) files published by the Centers for Medicare & Medicaid Services (CMS) for informational purposes only. The data is not an ICD-10 conversion tool and doesn’t guarantee clinical accuracy.

Similar Codes

ICD-10 Code ICD-10 Description
Q15 Other congenital malformations of eye
Q15.0 Congenital glaucoma
Q15.9 Congenital malformation of eye, unspecified


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