Progressive bifocal chorioretinal atrophy

disorder

SNOMED 719266007CUI C1833321

Overview

Progressive bifocal chorioretinal 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

Very frequent (80-99%)HP:0000565

Involuntary, rapid, rhythmic eye movements

Very frequent (80-99%)HP:0000639

Macular atrophy

Very frequent (80-99%)HP:0007401

Poor vision

Very frequent (80-99%)HP:0000505

Pigmentary retinopathy

Occasional (5-29%)HP:0000580

Chorioretinal atrophy

HP:0000533

Chorioretinal dystrophy

HP:0001135

Near sighted

HP:0000545

Retinal detachment

HP:0000541

Related Conditions

Autosomal dominant hereditary disorder(parent)

Hereditary retinal dystrophy(parent)

Chorioretinal degeneration(parent)

Quick Facts

SNOMED CT: 719266007
UMLS CUI: C1833321
Fully Specified Name: Progressive bifocal chorioretinal atrophy (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 9

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.