Iridocorneal endothelial syndrome

disorder

SNOMED 129623003CUI C1096100

Overview

Iridocorneal endothelial syndrome is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Signs & Symptoms

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

Abnormal migration of corneal endothelium

Frequent (30-79%)HP:0011489

Corectopia

Frequent (30-79%)HP:0009918

Corneal stromal edema

Frequent (30-79%)HP:0012040

Decreased visual acuity

Frequent (30-79%)HP:0007663

Decreased visual acuity, progressive

Frequent (30-79%)HP:0000529

Glaucoma

Frequent (30-79%)HP:0000501

Iridocorneal adhesions

Frequent (30-79%)HP:0011483

Iris atrophy

Frequent (30-79%)HP:0001089

Abnormal pupil shape

Occasional (5-29%)HP:0025309

Hypoplastic iris stroma

Occasional (5-29%)HP:0007990

Iris nevus

Occasional (5-29%)HP:0011525

Polycoria

Occasional (5-29%)HP:0011500

Posterior synechiae

Occasional (5-29%)HP:0011484

Ring iris heterochromia

Occasional (5-29%)HP:0007818

Uveal ectropion

Occasional (5-29%)HP:0025358

Heterochromia iridis

Very rare (1-4%)HP:0001100

Related Conditions

Cogan-Reese syndrome(child)

Essential iris atrophy(child)

Iridocorneal endothelial syndrome of left eye(child)

Iridocorneal endothelial syndrome of right eye(child)

Chandler syndrome(parent)

Quick Facts

SNOMED CT: 129623003
UMLS CUI: C1096100
Fully Specified Name: Iridocorneal endothelial syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 16

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.