Fuchs' corneal dystrophy

disorder

SNOMED 193839007CUI C0016781

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.

Abnormal corneal endothelium morphology

Very frequent (80-99%)HP:0011488

Abnormality of Descemet's membrane

Very frequent (80-99%)HP:0011490

Decreased visual acuity

Very frequent (80-99%)HP:0007663

Reduced number of corneal endothelial cells

Very frequent (80-99%)HP:0011491

Scarring or clouding of the cornea of the eye

Very frequent (80-99%)HP:0007957

Soft tissue swelling

Very frequent (80-99%)HP:0000969

Eye movement-induced pain

Frequent (30-79%)HP:0030857

Night blindness

Frequent (30-79%)HP:0000662

Visual loss

Frequent (30-79%)HP:0000572

Related Conditions

Chandler syndrome(parent)

Quick Facts

SNOMED CT: 193839007
UMLS CUI: C0016781
Fully Specified Name: Fuchs' corneal dystrophy (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.