9C61.42ICD-11 MMS 2026-01
Secondary childhood glaucoma
Index terms
- Secondary childhood glaucoma
- Glaucoma associated with congenital anomalies of the eye
- Goniodysgenesis, Axenfeld Rieger syndrome and Peters anomaly
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- ARS - [Axenfeld-Rieger spectrum]
- Peters anomaly
- Microspherophakia or Weill Marchesani Syndrome
- Macrocornea with glaucoma
- Megalocornea with glaucoma
- Macrophthalmos in congenital glaucoma
- Congenital keratoglobus with glaucoma
- Congenital Glaucoma associated with systemic disorders
- Childhood Glaucoma associated with systemic disorders
- Developmental Glaucoma associated with systemic disorders
- Congenital glaucoma associated with Sturge Weber syndrome
- Congenital glaucoma associated with homocystinuria
- Congenital glaucoma associated with chromosomal abnormalities
- Congenital glaucoma associated with Pierre Robin syndrome
- Secondary childhood glaucoma after congenital cataract surgery
Exclusions from above levels
Sibling codes
Foundation entity
Secondary childhood glaucoma – http://id.who.int/icd/entity/535678210
Allowed postcoordination axes
Part of: 9C61.4: Developmental glaucoma › 9C61: Glaucoma › 09: Diseases of the visual system