Q15.8
BillableOther specified congenital malformations of eye
Other specified congenital malformations of eye
Coding 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 metabolismE70-E88
- •cleft lip and cleft palateQ35-Q37
- •congenital malformation of cervical spine, , ,Q05.0, Q05.5, Q67.5, Q76.0-Q76.4
- •congenital malformation of larynxQ31
- •congenital malformation of lip NECQ38.0
- •congenital malformation of noseQ30
- •congenital malformation of parathyroid glandQ89.2
- •congenital malformation of thyroid glandQ89.2
Related Codes(2)
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(207)
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
Clinical Terms
- Unilateral diplophthalmia
- Congenital ocular melanocytosis of both eyes
- Bilateral congenital ocular melanocytosis of eyes
- Congenital proptosis
- Preauricular tag
- Port-wine stain with associated anomalies
- Congenital exophthalmos
- Extra nipple
- Abnormal eye movement
- Congenital ocular melanocytosis of left eye
- Megalocornea with intellectual disability syndrome
- Rotational orbital dystopia
- Triopia
- Horizontal orbital dystopia
- Bilateral congenital epibulbar choristoma
- MGCN - Megalocornea
- Isolated congenital megalocornea
- Congenital macrocornea
- Congenital vascular anomaly of eye
- Preauricular lobule
- Left epibulbar choristoma
- Developmental malformation of branchial arch
- Glaucoma due to congenital chamber angle anomaly
- Hyperthelia
- Melanosis oculi of right eye
- Supernumerary external ear
- Accessory auricle of ear
- Neuhäuser syndrome
- Congenital ocular melanocytosis of right eye
- Right epibulbar choristoma
- Atypical Norrie disease due to monosomy Xp11.3
- Atrophia bulborum hereditaria
- Supernumerary breast
- Ectopic nipple
- Congenital anterior megalophthalmia
- Congenital fibrosis syndrome
- Polythelia
- Spondyloocular syndrome
- Polyotia
- Polymastia
- Accessory breast
- Breast in the wrong place
- Preauricular appendage
- MMR (megalocornea, mental retardation) syndrome
- Choristoma of eye proper
- Enlarged cornea
- Hamartoma of retina
- Epibulbar choristoma
- Oligophrenia microphthalmus
- Congenital exophthalmia
- Cornea enlarged
- Bilateral megalocornea
- Congenital failure of eye elevation
- Congenital malpositioned eye
- Megalocornea of bilateral eyes
- Polymazia
- Choristoma of left eye proper
- Anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome
- Accessory auricle
- Glaucoma due to congenital malformation of angle of anterior chamber of eye
- Norrie's disease
- Cassia Stocco dos Santos syndrome
- Bilateral congenital anomaly of corneas
- Triophthalmia
- Congenital ocular melanocytosis of bilateral eyes
- Ocular melanosis
- Phakomatosis pigmentovascularis
- Accessory nipple
- Congenital structural abnormality of bilateral corneas
- Melanosis oculi
- Orbital dystopia
- Congenital structural abnormality of right cornea
- Unilateral ocular duplication
- Vertical orbital dystopia
- Melanosis oculi of bilateral eyes
- Melanosis oculi of left eye
- Congenital epibulbar choristoma of bilateral eyes
- Congenital anomaly of both corneas
- Spondylo-ocular syndrome
- Congenital structural abnormality of left cornea
- Hamartoma of retina of right eye
- Congenital fibrosis of extraocular muscles
- Congenital accessory nipple
- Congenital fibrosis of inferior rectus muscle
- Abnormal ocular motility
- Unilateral diplophthalmos
- Megalocornea of both eyes
- Megalocornea
- Atypical Norrie disease due to Xp11.3 microdeletion
- Epibulbar lipodermoid, preauricular appendage, polythelia syndrome
- Ectopic breast
- Congenital megalocornea
- Supernumerary ear
- Melanin pigmentation of eye
- Accessory tragus
- Congenital anomaly of bilateral corneas
- Congenital malposition of eye
- Hypoplasia of eye muscle
- Port-wine stain with oculocutaneous melanosis
- Ocular melanocytosis
- Supernumerary nipple
- Extraocular muscle restriction
- Choristoma of right eye proper
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.
How does Q15.8 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other specified congenital malformations of eye affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.
What is the ICD-11 equivalent of Q15.8?
Q15.8 maps to the ICD-11 code: LA1Z (Structural developmental anomalies of the eye, eyelid or lacrimal apparatus, unspecified).
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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.