Bradyopsia

disorder

SNOMED 711163009CUI C1842073

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.

Impaired vision

Very frequent (80-99%)HP:0000505

Photophobia

Very frequent (80-99%)HP:0000613

Related Conditions

Hereditary disorder of the visual system(parent)

Recessive hereditary disorder (autosomal)(parent)

Disorder of eye(parent)

Quick Facts

SNOMED CT: 711163009
UMLS CUI: C1842073
Fully Specified Name: Bradyopsia (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 2

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.