LA13.3

ICD-11 MMS 2026-01

Congenital vitreoretinal dysplasia

Description

Any disease caused by the maldevelopment of the vitreous and retina.

Index terms

  • Congenital vitreoretinal dysplasia
  • Familial exudative vitreoretinopathy
  • Criswick-Schepens syndrome
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  • FEVR - [familial exudative vitreoretinopathy]
  • Teratogenic congenital retinal dysplasia
  • Genetic congenital retinal dysplasia
  • Congenital anomaly of retina
  • congenital malformation of retina
  • Anomaly of fovea centralis
  • fovea centralis aplasia
  • Anomaly of retinal artery
  • Congenital hypoplasia of retinal artery
  • hypoplasia of retinal artery
  • Congenital stricture of retinal artery
  • Displacement of macula
  • macular displacement
  • Medullated fibres of retina
  • Congenital retinoschisis
  • Congenital pigmentation of retina

Exclusions from above levels

  • http://id.who.int/icd/entity/733825440 – Inborn errors of metabolism

Foundation children elsewhere

Sibling codes

  • LA13.0 – Congenital anomalies of the vitreous
  • LA13.1 – Coloboma of choroid or retina
  • LA13.2 – Coloboma of macula
  • LA13.5 – Congenital retinal aneurysm
  • LA13.6 – Congenital malformations of choroid
  • LA13.7 – Congenital malformation of optic disc
  • LA13.8 – Certain congenital malformations of posterior segment of eye
  • LA13.Y – Other specified structural developmental anomalies of the posterior segment of eye
  • LA13.Z – Structural developmental anomalies of the posterior segment of eye, unspecified

Foundation entity

Congenital vitreoretinal dysplasia – http://id.who.int/icd/entity/44221751

Allowed postcoordination axes

Part of: LA13: Structural developmental anomalies of the posterior segment of eye › 20: Developmental anomalies