Keratitis fugax hereditaria

disorder

SNOMED 1336030008CUI C1835697

Overview

Keratitis fugax hereditaria 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.

Corneal inflammation

Always present (100%)HP:0000491

Cloudy cornea

Frequent (30-79%)HP:0007759

Macular pucker

Occasional (5-29%)HP:0100014

Blurred vision

HP:0000622

Conjunctival hyperemia

HP:0030953

Increased lacrimation

HP:0009926

Photophobia

HP:0000613

Related Conditions

Autosomal dominant hereditary disorder(parent)

Hereditary disorder of immune system(parent)

Hereditary disorder of the visual system(parent)

Autoinflammatory syndrome(parent)

Recurrent disease(parent)

Keratitis(parent)

Quick Facts

SNOMED CT: 1336030008
UMLS CUI: C1835697
Fully Specified Name: Keratitis fugax hereditaria (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 7

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.