Irido-corneo-trabecular dysgenesis

disorder

SNOMED 204153003CUI C0344559

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.

Peters anomaly

Always present (100%)HP:0000659

Central opacification of the cornea

Very frequent (80-99%)HP:0011493

Corneal stromal opacity

Very frequent (80-99%)HP:0007759

Iridocorneal adhesions

Very frequent (80-99%)HP:0011483

Subcapsular opacities

Very frequent (80-99%)HP:0000523

Thinning of Descemet membrane

Very frequent (80-99%)HP:0031159

Infantile glaucoma

Frequent (30-79%)HP:0001087

Involuntary, rapid, rhythmic eye movements

Very rare (1-4%)HP:0000639

Squint

Very rare (1-4%)HP:0000486

Related Conditions

Congenital anomaly of anterior segment of eye(parent)

Quick Facts

SNOMED CT: 204153003
UMLS CUI: C0344559
Fully Specified Name: Irido-corneo-trabecular dysgenesis (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 9

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.