Cone dystrophy with supernormal rod response

disorder

SNOMED 719455002CUI C1835897

Overview

Cone dystrophy with supernormal rod response 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.

Macular atrophy

Occasional (5-29%)HP:0007401

Squint

Occasional (5-29%)HP:0000486

Abnormal curving of the cornea or lens of the eye

HP:0000483

Blind spot

HP:0000575

Cone-rod retinal dystrophy

HP:0000548

Decreased visual acuity

HP:0007663

Difficulties with night vision

HP:0000662

Horizontal nystagmus

HP:0000666

Near sighted

HP:0000545

Photophobia

HP:0000613

Related Conditions

Recessive hereditary disorder (autosomal)(parent)

Cone dystrophy(parent)

Quick Facts

SNOMED CT: 719455002
UMLS CUI: C1835897
Fully Specified Name: Cone dystrophy with supernormal rod response (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 10

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.