Overview
Retinitis punctata albescens 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.
Abnormal light- and dark-adapted electroretinogram
Very frequent (80-99%)HP:0008323
Decreased visual acuity, progressive
Very frequent (80-99%)HP:0000529
Loss of foveal reflex
Very frequent (80-99%)HP:0030825
Night blindness
Very frequent (80-99%)HP:0000662
Yellow/white lesions of the retina
Very frequent (80-99%)HP:0030506
Attenuation of retinal blood vessels
Frequent (30-79%)HP:0007843
Blind spot located at fixation point
Frequent (30-79%)HP:0000603
Kalnienk vision
Frequent (30-79%)HP:0007994
Photophobia
Frequent (30-79%)HP:0000613
Progressive night blindness
Frequent (30-79%)HP:0007675
Progressive visual field defects
Frequent (30-79%)HP:0007987
RPE irregularity
Frequent (30-79%)HP:0007814
Abnormality of fundus pigmentation
Occasional (5-29%)HP:0031605
Congenital neurosensory deafness
Occasional (5-29%)HP:0008527
Cystoid macular edema
Occasional (5-29%)HP:0011505
Lenticonus
Occasional (5-29%)HP:0001142
Macular atrophy
Occasional (5-29%)HP:0007401
Retinal atrophy
Occasional (5-29%)HP:0001105
Pigmentary retinal deposits
Very rare (1-4%)HP:0000580
Fundus albipunctatus
HP:0030642
Retinal flecks
HP:0012045
Quick Facts
- SNOMED CT
- 715562001
- UMLS CUI
- C1405854
- Fully Specified Name
- Retinitis punctata albescens (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 21
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.