Autosomal dominant rhegmatogenous retinal detachment

disorder

SNOMED 773727009CUI C1836081

Overview

Autosomal dominant rhegmatogenous retinal detachment 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.

Rhegmatogenous retinal detachment

Frequent (30-79%)HP:0012230

Flat midface

Occasional (5-29%)HP:0011800

Hearing impairment

Occasional (5-29%)HP:0000365

Near sighted

HP:0000545

Optically empty vitreous

HP:0030663

Related Conditions

Hereditary disorder of the visual system(parent)

Autosomal dominant hereditary disorder(parent)

Rhegmatogenous retinal detachment(parent)

Quick Facts

SNOMED CT: 773727009
UMLS CUI: C1836081
Fully Specified Name: Autosomal dominant rhegmatogenous retinal detachment (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.

Autosomal dominant rhegmatogenous retinal detachment — Symptoms, Testing & Specialists | Ltrl | Healos