Decorin associated congenital stromal corneal dystrophy

disorder

SNOMED 702359002CUI C1864738

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.

Corneal dystrophy

Always present (100%)HP:0001131

Squint

Frequent (30-79%)HP:0000486

Band-shaped corneal dystrophy

Occasional (5-29%)HP:0007709

Glaucoma

Occasional (5-29%)HP:0000501

Corneal erosion

Excluded (<1%)HP:0200020

Decreased visual acuity, progressive

HP:0000529

Increased corneal thickness

HP:0011487

Photophobia

Excluded (<1%)HP:0000613

Related Conditions

Autosomal dominant hereditary disorder(parent)

Stromal corneal dystrophy(parent)

Connective tissue hereditary disorder(parent)

Hereditary corneal dystrophy(parent)

Congenital connective tissue disorder(parent)

Quick Facts

SNOMED CT: 702359002
UMLS CUI: C1864738
Fully Specified Name: Congenital stromal corneal dystrophy (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 8

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.