Q14.1
BillableCongenital malformation of retina
Congenital malformation of retina
Status
Billable / Specific
Parent Code
Q14Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Congenital retinal aneurysm
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)
- optic nerve hypoplasia (H47.03-)
Also Known As / Clinical Terms
SNOMED CT
- Congenital retinal aneurysm943003
- Retinal haemangioblastomatosis2167004
- Retinal hemangioblastomatosis2167004
- Congenital vascular anomaly of eye2818004
- Congenital anomaly of macula4041005
- Congenital chorioretinal degeneration24210004
- Cornea small26098002
- Microcornea26098002
- Congenital anomaly of retina49381001
- Congenital malformation of retina49381001
- Congenital supravalvular pulmonary stenosis52757001
- Congenital hallux valgus53842005
- Albinotic fundus55819001
- Depigmentation of fundus55819001
- Congenital nystagmus64635004
- Juvenile retinoschisis86923008
- X-linked foveal retinoschisis86923008
- X-linked retinoschisis86923008
- Congenital retinoschisis95493003
- Retinal dysplasia95494009
- Multifocal retinal dysplasia95495005
- Persistent retinal folds95495005
- Geographic retinal dysplasia95496006
- Diffuse retinal dysplasia95497002
- Congenital arteriovenous malformation of retina95501007
- Congenital retinal arteriovenous anastomoses95501007
- Congenital retinal arteriovenous communication95501007
- Retinal arteriovenous anomaly95501007
- Retinal arteriovenous malformation95501007
- Chorioretinal atrophy95686007
- Coloboma of retina204173008
- Congenital retinal fold204181009
- Coloboma of choroid204192005
- Autosomal recessive medullary cystic disease204958008
- Familial juvenile medullary cystic kidney disease204958008
- Familial juvenile nephronophthisis204958008
- Nephronophthisis204958008
- Macular retinoschisis232013002
- Macular and peripheral retinoschisis232014008
- Angiomatosis of retina232073009
- CHRPE - Congenital hypertrophy of retinal pigment epithelium232074003
- Congenital hyperplasia of retinal pigment epithelium232074003
- Congenital hypertrophy of retinal pigment epithelium232074003
- Loken Senior syndrome236531005
- Renal dysplasia and retinal aplasia236531005
- Retinal macroaneurysm247124009
- Retinal arteriovenous shunt247127002
- Retinal pigment deposits247141006
- Retinal pigmentation grouped247142004
- Pulmonary trunk stenosis253621008
- Peripheral retinoschisis361130009
- Brachydactyly syndrome type B389168002
- RPE hypertrophy425217005
- Retinal pigment epithelial hypertrophy425217005
- Congenital hypoplasia of fovea429449002
- Congenital hypoplasia of fovea centralis429449002
- Presenile cataract441622000
- Supravalvar pulmonary trunk stenosis448027004
- Congenital stenosis of pulmonary artery449125001
- Vitreoretinal dysplasia449866003
- Arthrogryposis with oculomotor limitation and electroretinal anomaly715217004
- Distal arthrogryposis type 5715217004
- Distal arthrogryposis with ophthalmoplegia715217004
- Oculomelic amyoplasia715217004
- X-linked retinal dysplasia715240000
- Microcornea with corectopia and macular hypoplasia syndrome716165003
- Coloboma of macula with brachydactyly type B syndrome717785002
- Sorsby syndrome717785002
- Oliver McFarlane syndrome719944006
- Trichomegaly with retina pigmentary degeneration and dwarfism syndrome719944006
- Macular coloboma, cleft palate, hallux valgus syndrome722463001
- Coloboma of macula737579002
- Congenital coloboma of macula lutea737579002
- FRAM - familial retinal arterial macroaneurysm764452004
- Familial retinal arterial macroaneurysm764452004
- RAMSVPS - retinal arterial macroaneurysm with supravalvular pulmonic stenosis764452004
- Retinal arterial macroaneurysm with supravalvular pulmonic stenosis764452004
- Coloboma of choroid and retina768932000
- Foveal hypoplasia with presenile cataract syndrome778042000
- O'Donnell Pappas syndrome778042000
- FHONDA (foveal hypoplasia, optic nerve decussation defect, anterior segment dysgenesis) syndrome782754006
- FHONDA syndrome782754006
- Foveal hypoplasia, optic nerve decussation defect, anterior segment dysgenesis syndrome782754006
- Bilateral coloboma of macula840456001
- Coloboma of bilateral maculae840456001
- Coloboma of both maculae840456001
- Congenital retinal dysplasia caused by teratogenic substance897559009
- Teratogenic congenital retinal dysplasia897559009
- Solitary CHRPE (congenital hypertrophy of retinal pigment epithelium)1142277007
- Solitary congenital hypertrophy of retinal pigment epithelium1142277007
- Unifocal CHRPE (congenital hypertrophy of retinal pigment epithelium)1142277007
- Congenital hypoplasia of retina1144397003
- Congenital retinal hypoplasia1144397003
- Congenital hypoplasia of macula lutea1144408000
- Congenital macular hypoplasia1144408000
- Congenital peripapillary staphyloma1230020008
- Isolated foveal hypoplasia1231150005
- Isolated hypoplasia of fovea centralis1231150005
- Extensive peripapillary myelinated nerve fibers of retina1237337007
- Extensive peripapillary myelinated nerve fibres of retina1237337007
- Myelinated nerve fiber layer of retina1237370002
- Myelinated nerve fibre layer of retina1237370002
- Bilateral choroid degeneration346911000119103
- Choroid degeneration of bilateral eyes346911000119103
- Choroid degeneration of both eyes346911000119103
- Bilateral congenital anomaly of retinas15986791000119106
- Congenital anomaly of bilateral retinas15986791000119106
- Congenital anomaly of both retinas15986791000119106
- Bilateral congenital hypertrophy of retinal pigment epithelium15986551000119109
- Congenital bear track retinal pigment hypertrophy of bilateral eyes15986551000119109
- Congenital hypertrophy of retinal pigment epithelium of bilateral eyes15986551000119109
- Congenital hypertrophy of retinal pigment epithelium of both eyes15986551000119109
- Congenital anomaly of left retina15986751000119101
- Congenital anomaly of retina of left eye15986751000119101
- Congenital anomaly of retina of right eye15986471000119104
- Congenital anomaly of right retina15986471000119104
- Congenital bear track retinal pigment hypertrophy of left eye15986591000119104
- Congenital hypertrophy of retinal pigment epithelium of left eye15986591000119104
- Congenital bear track retinal pigment hypertrophy of right eye15986511000119108
- Congenital hypertrophy of retinal pigment epithelium of right eye15986511000119108
- Congenital chorioretinal degeneration of bilateral eyes15986351000119102
- Congenital chorioretinal degeneration of both eyes15986351000119102
- Congenital chorioretinal degeneration of left eye15986431000119102
- Congenital chorioretinal degeneration of right eye15986391000119107
Frequently Asked Questions
What is the ICD-10 code for congenital malformation of retina?
The ICD-10-CM code for congenital malformation of retina is Q14.1. The full clinical description is "Congenital malformation of retina". Q14.1 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q14.1 mean?
ICD-10-CM code Q14.1 represents "Congenital malformation of retina". 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 Q14.1 a billable code?
Yes, Q14.1 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q14.1 in?
Q14.1 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What SNOMED CT codes does Q14.1 map to?
Q14.1 maps to 71 SNOMED CT concepts: 55819001, 232073009, 715217004, 204958008, 346911000119103, and 66 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q14.1?
Q14.1 is linked to 2 UMLS Concept Unique Identifiers: C0266564, C0266571. 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.