Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Cystoid macular edema
Very frequent (80-99%)HP:0011505
Intraretinal haemorrhage
Very frequent (80-99%)HP:0031805
Macular cotton wool spot
Very frequent (80-99%)HP:0030497
Macular oedema
Frequent (30-79%)HP:0040049
Papillitis
Frequent (30-79%)HP:0001085
Tortuous retinal vessels
Frequent (30-79%)HP:0012841
Visual loss
Frequent (30-79%)HP:0000572
Abnormality of the anterior segment of the globe
Occasional (5-29%)HP:0004328
Blurred vision
Occasional (5-29%)HP:0000622
Electronegative ERG
Occasional (5-29%)HP:0007984
Glaucoma
Occasional (5-29%)HP:0000501
Large central loss of field of vision
Occasional (5-29%)HP:0001129
Macular pucker
Occasional (5-29%)HP:0100014
Pigmentary retinal deposits
Occasional (5-29%)HP:0000580
Pigmented macular degeneration
Occasional (5-29%)HP:0000608
Retinal neovascularisation
Occasional (5-29%)HP:0030666
Related Conditions
Central retinal vein occlusion with neovascularisation(child)
Central retinal vein occlusion with macular edema(child)
Central retinal vein occlusion in young adults(child)
Central retinal vein occlusion - ischaemic(child)
Central retinal vein occlusion - non-ischemic(child)
Thrombosis of retinal vein(parent)
Retinal vascular occlusion(parent)
Venous occlusion(parent)
Occlusion of retinal vein(parent)
Quick Facts
- SNOMED CT
- 68478007
- UMLS CUI
- C0154841
- Fully Specified Name
- Central retinal vein occlusion (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 16
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.