Pigmented paravenous retinochoroidal atrophy

disorder

SNOMED 723450004CUI C1868310

Overview

Pigmented paravenous retinochoroidal atrophy 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.

Esotropia

HP:0000565

Fundus with peripheral bony spicules

HP:0007737

Hyperopia

HP:0000540

Paravenous chorioretinal atrophy

HP:0007903

Vitreoretinopathy

HP:0007773

Related Conditions

Congenital disease(parent)

Chorioretinal atrophy(parent)

Hereditary disorder of the visual system(parent)

Quick Facts

SNOMED CT: 723450004
UMLS CUI: C1868310
Fully Specified Name: Pigmented paravenous retinochoroidal atrophy (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 5

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.