Diagnosis Code: Q14.1

Short Description: Congenital malformation of retina

Long Description: Congenital malformation of retina

The code Q14.1 is VALID for claim submission

Code Classification:

• Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
  • Congenital malformations of eye, ear, face and neck (Q10-Q18)
    • Congenital malformations of posterior segment of eye (Q14)
      • Q14.1 Congenital malformation of retina

Code Version: 2022 ICD-10-CM

Synonyms

• Albinotic fundus
• Angiomatosis of retina
• Arthrogryposis with oculomotor limitation and electroretinal anomaly
• Bilateral coloboma of macula
• Bilateral congenital anomaly of retinas
• Bilateral congenital hypertrophy of retinal pigment epithelium
• Brachydactyly syndrome type B
• Chorioretinal atrophy
• Coloboma of choroid
• Coloboma of choroid and retina
• Coloboma of macula with brachydactyly type B syndrome
• Coloboma of retina
• Congenital anomaly of left retina
• Congenital anomaly of macula
• Congenital anomaly of macula
• Congenital anomaly of macula
• Congenital anomaly of macula
• Congenital anomaly of macula
• Congenital anomaly of retina
• Congenital anomaly of right retina
• Congenital chorioretinal degeneration
• Congenital coloboma of macula lutea
• Congenital coloboma of macula lutea
• Congenital coloboma of macula lutea
• Congenital hallux valgus
• Congenital hypertrophy of retinal pigment epithelium
• Congenital hypertrophy of retinal pigment epithelium of left eye
• Congenital hypertrophy of retinal pigment epithelium of right eye
• Congenital hypoplasia of fovea centralis
• Congenital hypoplasia of fovea centralis
• Congenital hypoplasia of fovea centralis
• Congenital malformation of vitreous humor
• Congenital nystagmus
• Congenital peripapillary staphyloma
• Congenital retinal aneurysm
• Congenital retinal aneurysm
• Congenital retinal dysplasia caused by teratogenic substance
• Congenital retinal fold
• Congenital retinoschisis
• Congenital stenosis of pulmonary artery
• Congenital supravalvular pulmonary stenosis
• Congenital vascular anomaly of eye
• Congenital vascular anomaly of eye
• Congenital vascular anomaly of eye
• Diffuse retinal dysplasia
• Extensive peripapillary myelinated nerve fibers of retina
• Foveal hypoplasia with presenile cataract syndrome
• Foveal hypoplasia, optic nerve decussation defect, anterior segment dysgenesis syndrome
• Geographic retinal dysplasia
• Isolated foveal hypoplasia
• Juvenile retinoschisis
• Macular and peripheral retinoschisis
• Macular coloboma, cleft palate, hallux valgus syndrome
• Macular retinoschisis
• Microcornea
• Microcornea with corectopia and macular hypoplasia syndrome
• Multifocal retinal dysplasia
• Myelinated nerve fiber layer of retina
• Nephronophthisis
• Oliver McFarlane syndrome
• Peripheral retinoschisis
• Presenile cataract
• Pulmonary trunk stenosis
• Renal dysplasia and retinal aplasia
• Retinal arterial macroaneurysm with supravalvular pulmonic stenosis
• Retinal arteriovenous malformation
• Retinal arteriovenous shunt
• Retinal dysplasia
• Retinal dysplasia
• Retinal dysplasia
• Retinal hemangioblastomatosis
• Retinal macroaneurysm
• Retinal pigment deposits
• Retinal pigment epithelial hypertrophy
• Retinal pigment epithelial hypertrophy
• Retinal pigment epithelial hypertrophy
• Retinal pigment epithelial hypertrophy
• Retinal pigmentation grouped
• Supravalvar pulmonary trunk stenosis
• Vitreoretinal dysplasia
• X-linked retinal dysplasia

Diagnostic Related Group(s)

The code Q14.1 is grouped in the following Diagnostic Related Group(s) (MS-DRG v39.0)

• Other Disorders Of The Eye With Mcc Or Thrombolytic Agent (124)
• Other Disorders Of The Eye Without Mcc (125)

References to Index of Diseases and Injuries

The code Q14.1 has the following ICD-10-CM references to the Index of Diseases and Injuries

• Inclusion Terms:
  • Congenital retinal aneurysm

Crosswalk Information

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This page was last updated on: 10/1/2023

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