Glaucoma of childhood

disorder

SNOMED 71111008CUI C2981140

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Abnormality iris morphology

Frequent (30-79%)HP:0000525

Anterior chamber anomalies

Frequent (30-79%)HP:0000593

Damaged optic nerve

Frequent (30-79%)HP:0001138

Elevated IOP

Frequent (30-79%)HP:0007906

Glaucomatous visual field defect

Frequent (30-79%)HP:0007854

Kalnienk vision

Frequent (30-79%)HP:0007994

Open angle glaucoma

Frequent (30-79%)HP:0012108

optic nerve abnormalities

Frequent (30-79%)HP:0000587

Poor vision

Frequent (30-79%)HP:0000505

Increased cup-to-disc ratio

Occasional (5-29%)HP:0012796

Severe myopia

Occasional (5-29%)HP:0011003

Temporal optic disc pallor

Occasional (5-29%)HP:0012511

Central scotoma

Very rare (1-4%)HP:0000603

Retinal arterial occlusion

Very rare (1-4%)HP:0025326

Retinal vein occlusion

Very rare (1-4%)HP:0012636

Related Conditions

Secondary childhood glaucoma after congenital cataract surgery(child)

Glaucoma(parent)

Quick Facts

SNOMED CT: 71111008
UMLS CUI: C2981140
Fully Specified Name: Glaucoma of childhood (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 15

Medical Disclaimer

This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.

Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.