Goldmann-Favre syndrome

disorder

SNOMED 232065000CUI C0339541

Overview

Goldmann-Favre syndrome 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.

Abolished electroretinogram

HP:0000550

Difficulties with night vision

HP:0000662

Hemeralopia

HP:0012047

Lens opacities

HP:0000518

Macular oedema

HP:0040049

Retinal pigmentary degeneration

HP:0000580

Retinoschisis

HP:0030502

Vitreoretinopathy

HP:0007773

Water retention

HP:0000969

Related Conditions

Chronic disease of ocular adnexa(parent)

Connective tissue hereditary disorder(parent)

Vitreous degeneration(parent)

Vitreoretinal dystrophy(parent)

Recessive hereditary disorder (autosomal)(parent)

Quick Facts

SNOMED CT: 232065000
UMLS CUI: C0339541
Fully Specified Name: Goldmann-Favre syndrome (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.