ICD-11 classes
20 Developmental anomalies
Structural developmental anomalies primarily affecting one...
Structural developmental anomalies of the eye, eyelid or...
LA11 — Structural developmental anomalies of the anterior segment...
9C61.4 — Developmental glaucoma
9C61.42 — Secondary childhood glaucoma
5C60.0 — Oculocerebrorenal syndrome
ICD-11 5C60.0 — Oculocerebrorenal syndrome
Oculocerebrorenal syndrome of Lowe (OCRL) is a multisystem disorder characterised by congenital cataracts, glaucoma, intellectual disabilities, postnatal growth retardation and renal tubular dysfunction with chronic renal failure.
The diagnosis includes nothing.
The diagnosis excludes nothing.
It has no clarifying diagnoses.
The diagnosis is coded elsewhere:
- Disorders of amino acid absorption or transport #4948
- Fanconi syndrome #4952
- Secondary childhood glaucoma #9882
- Secondary childhood glaucoma #10480
- Fanconi syndrome #19682
- Syndromes with multiple structural anomalies, not of environmental origin #23437
- Conditions with disorders of intellectual development as a relevant clinical feature #23735