Polymorphous corneal dystrophy

disorder

SNOMED 29504002CUI C0339284

Overview

Polymorphous corneal dystrophy 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.

Abnormality of Descemet's membrane

Very frequent (80-99%)HP:0011490

Reduced number of corneal endothelial cells

Very frequent (80-99%)HP:0011491

Abnormal curving of the cornea or lens of the eye

Occasional (5-29%)HP:0000483

Corectopia

Occasional (5-29%)HP:0009918

Corneal stromal edema

Occasional (5-29%)HP:0012040

Decreased visual acuity

Occasional (5-29%)HP:0007663

Increased corneal curvature

Occasional (5-29%)HP:0100692

Iridocorneal adhesions

Occasional (5-29%)HP:0011483

Iris atrophy

Occasional (5-29%)HP:0001089

Thinning of Descemet membrane

Occasional (5-29%)HP:0031159

Uveal ectropion

Occasional (5-29%)HP:0025358

Very low visual acuity

Occasional (5-29%)HP:0032122

Wandering eye

Occasional (5-29%)HP:0000646

Abnormality of tear production

Very rare (1-4%)HP:0000632

Blurred vision

Very rare (1-4%)HP:0000622

Chorioretinal atrophy

Very rare (1-4%)HP:0000533

Elevated IOP

Very rare (1-4%)HP:0007906

Esotropia

Very rare (1-4%)HP:0000565

Eye pain

Very rare (1-4%)HP:0200026

Glaucoma

Very rare (1-4%)HP:0000501

Photophobia

Very rare (1-4%)HP:0000613

Scarring or clouding of the cornea of the eye

Very rare (1-4%)HP:0007957

Abnormal corneal endothelium morphology

HP:0011488

Band keratopathy

HP:0000585

Increased lacrimation

HP:0009926

Polymorphous posterior corneal dystrophy

HP:0007915

Related Conditions

Hereditary corneal dystrophy(parent)

Corneal endothelial dystrophy(parent)

Autosomal dominant hereditary disorder(parent)

Abnormality of Descemet membrane morphology(parent)

Quick Facts

SNOMED CT: 29504002
UMLS CUI: C0339284
Fully Specified Name: Posterior polymorphous corneal dystrophy (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 26

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.