Q14.8
BillableOther congenital malformations of posterior segment of eye
Other congenital malformations of posterior segment of eye
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Coloboma of the fundus
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
- •optic nerve hypoplasiaH47.03
Related Codes(5)
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(83)
SNOMED CT
- Cornea small26098002
- Microcornea26098002
- Coloboma of fundus39302008
- Fundus coloboma39302008
- Congenital cyst of posterior segment of eye62631009
- Congenital fold of posterior segment of eye65997000
- Posterior lenticonus95482000
- Congenital fold and cyst of posterior segment of eye204175001
- Coloboma of choroid204192005
- Cilioretinal vessels247210001
- Retinociliary vessels247210001
- Cilioretinal artery247211002
- Lenticonus253221000
- Cilioretinal artery sparing419786001
- Retinal collateral vessels422233000
- Retinal collaterals422233000
- Retinal vessel collaterals422233000
- Coloboma of choroid and retina768932000
- MPPC (microcornea, posterior megalolenticonus, persistent fetal vasculature, coloboma) syndrome773690008
- MPPC (microcornea, posterior megalolenticonus, persistent foetal vasculature, coloboma) syndrome773690008
- Microcornea, posterior megalolenticonus, persistent fetal vasculature, coloboma syndrome773690008
- Microcornea, posterior megalolenticonus, persistent foetal vasculature, coloboma syndrome773690008
- Bilateral congenital anomaly of retinas15986791000119106
- Congenital anomaly of bilateral retinas15986791000119106
- Congenital anomaly of both retinas15986791000119106
- Bilateral congenital chorioretinal coloboma of eyes15665401000119102
- Congenital chorioretinal coloboma of bilateral eyes15665401000119102
- Congenital chorioretinal coloboma of both eyes15665401000119102
- Congenital chorioretinal coloboma of left eye15665361000119106
- Left congenital chorioretinal coloboma15665361000119106
- Congenital chorioretinal coloboma of right eye15665321000119101
- Right congenital chorioretinal coloboma15665321000119101
UMLS
- Birth defect that causes a hole in the innermost layer at the back of the eyeC0240896
- Chorioretinal colobomaC0240896
- Chorioretinal colobomasC0240896
- Choroidoretinal colobomaC0240896
- Coloboma of fundusC0240896
- Coloboma of the fundusC0240896
- Coloboma, chorioretinalC0240896
- Coloboma, retinochoroidalC0240896
- Fundus colobomaC0240896
- Fundus coloboma (disorder)C0240896
- Other congenital malformations of posterior segment of eyeC0477985
Clinical Terms
- Bilateral congenital chorioretinal coloboma of eyes
- Right congenital chorioretinal coloboma
- Coloboma of the fundus
- Cilioretinal artery sparing
- Congenital chorioretinal coloboma of both eyes
- Retinal vessel collaterals
- Congenital fold and cyst of posterior segment of eye
- Birth defect that causes a hole in the innermost layer at the back of the eye
- Cilioretinal artery
- Congenital anomaly of both retinas
- Coloboma, retinochoroidal
- Left congenital chorioretinal coloboma
- Retinal collateral vessels
- Congenital chorioretinal coloboma of left eye
- Chorioretinal coloboma
- Fundus coloboma
- Congenital chorioretinal coloboma of bilateral eyes
- Chorioretinal colobomas
- Fundus coloboma (disorder)
- Choroidoretinal coloboma
- Cornea small
- Congenital chorioretinal coloboma of right eye
- Cilioretinal vessels
- Microcornea, posterior megalolenticonus, persistent foetal vasculature, coloboma syndrome
- Retinal collaterals
- Coloboma of fundus
- Retinociliary vessels
- MPPC (microcornea, posterior megalolenticonus, persistent foetal vasculature, coloboma) syndrome
- Lenticonus
- Microcornea
- Coloboma of choroid
- Coloboma, chorioretinal
- Congenital fold of posterior segment of eye
- Microcornea, posterior megalolenticonus, persistent fetal vasculature, coloboma syndrome
- Congenital anomaly of bilateral retinas
- Coloboma of choroid and retina
- Congenital cyst of posterior segment of eye
- Posterior lenticonus
- MPPC (microcornea, posterior megalolenticonus, persistent fetal vasculature, coloboma) syndrome
- Bilateral congenital anomaly of retinas
Frequently Asked Questions
What is the ICD-10 code for other congenital malformations of posterior segment of eye?
The ICD-10-CM code for other congenital malformations of posterior segment of eye is Q14.8. The full clinical description is "Other congenital malformations of posterior segment of eye". Q14.8 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q14.8 mean?
ICD-10-CM code Q14.8 represents “Other congenital malformations of posterior segment 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 Q14.8 a billable code?
Yes, Q14.8 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q14.8 in?
Q14.8 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What SNOMED CT codes does Q14.8 map to?
Q14.8 maps to 18 SNOMED CT concepts: 15986791000119106, 15665401000119102, 247211002, 419786001, 247210001, and 13 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q14.8?
Q14.8 is linked to 2 UMLS Concept Unique Identifiers: C0240896, C0477985. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does Q14.8 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other congenital malformations of posterior segment 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 Q14.8?
Q14.8 maps to the ICD-11 code: LA13.Z (Structural developmental anomalies of the posterior segment of eye, 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.