Q15.8
BillableOther specified congenital malformations of eye
Other specified congenital malformations of eye
Status
Billable / Specific
Parent Code
Q15Coding Notes
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Excludes 2
Conditions not included here, but the patient may have both
- inborn errors of metabolism (E70-E88)
- 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)
Also Known As / Clinical Terms
SNOMED CT
- Congenital vascular anomaly of eye2818004
- Atrophia bulborum hereditaria15228007
- Norrie's disease15228007
- Oligophrenia microphthalmus15228007
- Accessory breast18166000
- Breast in the wrong place18166000
- Ectopic breast18166000
- Polymastia18166000
- Polymazia18166000
- Supernumerary breast18166000
- Accessory auricle35547002
- Accessory auricle of ear35547002
- Polyotia35547002
- Supernumerary ear35547002
- Supernumerary external ear35547002
- Melanosis oculi45795007
- Ocular melanocytosis45795007
- Ocular melanosis45795007
- Accessory nipple50956007
- Congenital accessory nipple50956007
- Ectopic nipple50956007
- Extra nipple50956007
- Hyperthelia50956007
- Polythelia50956007
- Supernumerary nipple50956007
- Congenital exophthalmia93081001
- Congenital exophthalmos93081001
- Congenital proptosis93081001
- Congenital malposition of eye93320008
- Congenital malpositioned eye93320008
- Abnormal eye movement103252009
- Abnormal ocular motility103252009
- Glaucoma due to congenital chamber angle anomaly193552006
- Glaucoma due to congenital malformation of angle of anterior chamber of eye193552006
- Hypoplasia of eye muscle204217005
- Accessory tragus204245004
- Preauricular appendage204245004
- Preauricular lobule204245004
- Preauricular tag204245004
- Congenital failure of eye elevation230529008
- Orbital dystopia253241005
- Horizontal orbital dystopia253242003
- Vertical orbital dystopia253243008
- Rotational orbital dystopia253244002
- Congenital macrocornea268158009
- Congenital megalocornea268158009
- Cornea enlarged268158009
- Enlarged cornea268158009
- MGCN - Megalocornea268158009
- Megalocornea268158009
- Congenital fibrosis of extraocular muscles400946004
- Congenital fibrosis syndrome400946004
- Congenital fibrosis of inferior rectus muscle400947008
- Developmental malformation of branchial arch402810002
- Port-wine stain with associated anomalies403544009
- Phakomatosis pigmentovascularis403545005
- Port-wine stain with oculocutaneous melanosis403545005
- Extraocular muscle restriction410504008
- Hamartoma of retina417125003
- Melanin pigmentation of eye421735009
- Spondylo-ocular syndrome715653007
- Spondyloocular syndrome715653007
- Anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome720495005
- Cassia Stocco dos Santos syndrome720495005
- MMR (megalocornea, mental retardation) syndrome733522005
- Megalocornea with intellectual disability syndrome733522005
- Neuhäuser syndrome733522005
- Atypical Norrie disease due to Xp11.3 microdeletion733626002
- Atypical Norrie disease due to monosomy Xp11.3733626002
- Congenital anterior megalophthalmia734026006
- Isolated congenital megalocornea734026006
- Choristoma of right eye proper830019003
- Right epibulbar choristoma830019003
- Choristoma of left eye proper830020009
- Left epibulbar choristoma830020009
- Choristoma of eye proper830021008
- Epibulbar choristoma830021008
- Bilateral megalocornea866089007
- Megalocornea of bilateral eyes866089007
- Megalocornea of both eyes866089007
- Bilateral congenital epibulbar choristoma890378005
- Congenital epibulbar choristoma of bilateral eyes890378005
- Epibulbar lipodermoid, preauricular appendage, polythelia syndrome1208480004
- Triophthalmia1285322008
- Triopia1285322008
- Unilateral diplophthalmia1285322008
- Unilateral diplophthalmos1285322008
- Unilateral ocular duplication1285322008
- Bilateral congenital anomaly of corneas15987551000119107
- Congenital anomaly of bilateral corneas15987551000119107
- Congenital anomaly of both corneas15987551000119107
- Congenital structural abnormality of bilateral corneas15987551000119107
- Bilateral congenital ocular melanocytosis of eyes13015821000119105
- Congenital ocular melanocytosis of bilateral eyes13015821000119105
- Congenital ocular melanocytosis of both eyes13015821000119105
- Melanosis oculi of bilateral eyes13015821000119105
- Congenital ocular melanocytosis of left eye13015741000119105
- Melanosis oculi of left eye13015741000119105
- Congenital ocular melanocytosis of right eye13015781000119100
- Melanosis oculi of right eye13015781000119100
- Congenital structural abnormality of left cornea15987511000119106
- Congenital structural abnormality of right cornea15987591000119102
- Hamartoma of retina of right eye15708121000119101
Frequently Asked Questions
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. The full clinical description is "Other specified congenital malformations of eye". Q15.8 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q15.8 mean?
ICD-10-CM code Q15.8 represents "Other specified congenital malformations of eye". It is classified under Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities and is a billable/specific code that can be used on a claim.
Is Q15.8 a billable code?
Yes, Q15.8 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q15.8 in?
Q15.8 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What codes cannot be used with Q15.8?
Q15.8 has Excludes1 notes indicating codes that cannot be used together with it, including: congenital nystagmus (H55.01); ocular albinism (E70.31-); optic nerve hypoplasia (H47.03-); and 1 more.
What SNOMED CT codes does Q15.8 map to?
Q15.8 maps to 45 SNOMED CT concepts: 103252009, 35547002, 18166000, 50956007, 204245004, and 40 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q15.8?
Q15.8 is linked to 1 UMLS Concept Unique Identifier: C0477986. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.