Autosomal dominant vitreoretinochoroidopathy

disorder

SNOMED 711162004CUI C3888099

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Dyschromatopsia

Occasional (5-29%)HP:0007641

Nanophthalmos

Occasional (5-29%)HP:0000568

Abnormality of chorioretinal pigmentation

HP:0007661

Color vision defects

HP:0000551

Congenital cataracts, bilateral

HP:0000519

Decreased corneal diameter

HP:0000482

Difficulties with night vision

HP:0000662

Glaucoma

HP:0000501

Involuntary, rapid, rhythmic eye movements

HP:0000639

Legal blindness

HP:0000618

Pigmentary retinal deposits

HP:0000580

Posterior staphyloma

HP:0030856

Pulverulent cataract

HP:0010693

Retinal arteriolar narrowing

HP:0008043

Retinal arteriolar occlusion

HP:0007985

Retinal detachment

HP:0000541

Retinal neovascularisation

HP:0030666

Squint

HP:0000486

Vitreous hemorrhage

HP:0007902

Related Conditions

Autosomal dominant hereditary disorder(parent)

Hereditary retinal dystrophy(parent)

Quick Facts

SNOMED CT: 711162004
UMLS CUI: C3888099
Fully Specified Name: Autosomal dominant vitreoretinochoroidopathy (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 19

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.