Helicoid peripapillary chorioretinal degeneration

disorder

SNOMED 724384008CUI C1862382

Overview

Helicoid peripapillary chorioretinal degeneration 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.

Abnormal curving of the cornea or lens of the eye

HP:0000483

Near sighted

HP:0000545

Peripapillary chorioretinal atrophy

HP:0007950

Related Conditions

Autosomal dominant hereditary disorder(parent)

Chorioretinal atrophy(parent)

Hereditary disorder of the visual system(parent)

Quick Facts

SNOMED CT: 724384008
UMLS CUI: C1862382
Fully Specified Name: Helicoid peripapillary chorioretinal degeneration (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 3

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.