2027 ICD-10-CM Diagnosis Code Q15.8Other specified congenital malformations of eye
ICD-10-CM Codes›Q00-Q99›Q10-Q18›Q15
- Billable — Valid for Submission
- POA Exempt
- Chronic Condition
Q15.8 is a billable ICD-10-CM diagnosis code for other specified congenital malformations of eye. It is valid on HIPAA claims for fiscal year 2027 (October 1, 2026 through September 30, 2027) and groups to MS-DRG 124 through 125. The code is exempt from POA reporting. In AHRQ's Clinical Classifications Software (CCSR), this diagnosis falls under Congenital malformations of eye, ear, face, neck.
Code Identity
Code Classification
Present on Admission (POA)Billing
Q15.8 is exempt from POA reporting on inpatient claims to general acute care hospitals. Review the other POA exempt codes in Congenital malformations of eye, ear, face and neck (Q10-Q18).
Approximate SynonymsGuidance
Alternate terms and clinical phrases that map to this code.
- 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 ocular melanocytosis of eyes
- Choristoma of eye proper
- Choristoma of left eye proper
- Choristoma of right eye proper
- 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 structural abnormality of bilateral corneas
- Congenital structural abnormality of left cornea
- Congenital structural abnormality of right cornea
- Congenital vascular anomaly of eye
- Developmental malformation of branchial arch
- Epibulbar lipodermoid, preauricular appendage, polythelia syndrome
- Extraocular muscle restriction
- Glaucoma due to congenital chamber angle anomaly
- Hamartoma of retina
- Hamartoma of retina of right eye
- Horizontal orbital dystopia
- Hypoplasia of eye muscle
- Isolated congenital megalocornea
- Megalocornea
- Megalocornea of bilateral eyes
- Megalocornea with intellectual disability syndrome
- 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
- Triopia
- Vertical orbital dystopia
Instructional NotesGuidance
Instructions from the official ICD-10-CM Tabular List that apply to Q15.8: its own notes plus those printed at Q15, block Q10-Q18, and Chapter 17. A note printed at a category, block or chapter applies to every code under it.
Excludes1
Not coded here: the excluded code is never reported together with this one, unless the two conditions are unrelated.
Excludes2
Not included here: the excluded condition is not part of this code, but a patient may have both, so both codes may be reported.
- cleft lip and cleft palate (Q35-Q37)
- congenital malformation of cervical spine (Q05.0, Q05.5, Q67.5, Q76.0-Q76.4)
- congenital malformation of larynx (Q31.-)
- congenital malformation of lip NEC (Q38.0)
- congenital malformation of nose (Q30.-)
- congenital malformation of parathyroid gland (Q89.2)
- congenital malformation of thyroid gland (Q89.2)
Notes
General instructions on how these codes are used.
- Codes from this chapter are not for use on maternal records
Source: CMS ICD-10-CM Tabular List. How to read instructional notes.
Index to Diseases and InjuriesGuidance
Alphabetical index entries that point to this code.
Aberrant (congenital) See Also: Malposition, congenital;
eye Q15.8
Anomaly, anomalous (congenital) (unspecified type) Q89.9
eye Q15.8
specified NEC Q15.8
ocular muscle Q15.8
eye Q15.8
eyeball (acquired) (lateral) (old) See: Displacement, globe;
congenital Q15.8
congenital Q15.8
congenital Q15.8
Macrocornea Q15.8
Malformation (congenital) See Also: Anomaly;
specified NEC Q15.8
eye Q15.8
Megalocornea Q15.8
congenital Q15.8
Clinical ClassificationClinical
AHRQ’s CCSR groups this code into broader clinical categories.
Patient EducationClinical
Birth Defects
A birth defect is a problem that happens while a baby is developing in the mother's body. Most birth defects happen during the first 3 months of pregnancy. One out of every 33 babies in the United States is born with a birth defect.
The full article covers:
- What are birth defects?
- What causes birth defects?
- Who is at risk of having a baby with birth defects?
- How are birth defects diagnosed?
- What are the treatments for birth defects?
- Can birth defects be prevented?
Read the full article at MedlinePlus
Courtesy of MedlinePlus, a service of the U.S. National Library of Medicine.
Convert Q15.8 to ICD-9-CMHistory
The closest ICD-9-CM equivalents under the General Equivalence Mappings.
Code HistoryHistory
Questions About Q15.8Overview
What is the ICD-10 code for other specified congenital malformations of eye?
The ICD-10-CM code for other specified congenital malformations of eye is Q15.8 (sometimes written as Q158). It is billable on HIPAA-covered claims from October 1, 2026 through September 30, 2027.
Is Q15.8 (Other congenital malformations of eye) a billable code?
Yes. This is a billable ICD-10-CM code, specific enough to report other specified congenital malformations of eye on HIPAA-covered claims from October 1, 2026 through September 30, 2027.
What MS-DRG does Q15.8 group to?
When other specified congenital malformations of eye is the principal diagnosis on an inpatient stay, it groups to MS-DRG 125, 124, with relative weights from 0.7699 to 1.2470 depending on complications. Higher weights mean higher Medicare reimbursement.
Is Q15.8 exempt from POA reporting?
Yes. CMS lists this code among those exempt from present on admission reporting, so hospitals do not assign a POA indicator for other specified congenital malformations of eye on inpatient claims. The code appears in the Congenital malformations of eye, ear, face and neck (Q10-Q18) range of the CMS exempt list.
Can Q15.8 be reported with H55.01?
Not as a rule. The Excludes1 note at Q15, which applies to Q15.8, lists "congenital nystagmus (H55.01)". An Excludes1 note means the excluded code is never reported together with this one; the only exception is when the two conditions are unrelated to each other (Official Guidelines, Section I.A.12.a).