Autosomal dominant neovascular inflammatory vitreoretinopathy

disorder

SNOMED 770791000CUI C4721549

Overview

Autosomal dominant neovascular inflammatory vitreoretinopathy 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.

Legal blindness

Always present (100%)HP:0000618

Abnormal ERG

HP:0000512

Large hyperpigmented retinal spots

HP:0007658

Peripheral retinal neovascularization

HP:0030667

Posterior retinal neovascularization

HP:0007778

Retinal detachment

HP:0000541

Uveitis

HP:0000554

Vitreoretinopathy

HP:0007773

Vitreous hemorrhage

HP:0007902

Related Conditions

Vitreoretinal degeneration(parent)

Hereditary disorder of the visual system(parent)

Autosomal dominant hereditary disorder(parent)

Chronic disease of ocular adnexa(parent)

Connective tissue hereditary disorder(parent)

Quick Facts

SNOMED CT: 770791000
UMLS CUI: C4721549
Fully Specified Name: Autosomal dominant neovascular inflammatory vitreoretinopathy (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.