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Central areolar choroidal sclerosis

disorder
SNOMED 231996009CUI C1536451

Overview

Central areolar choroidal sclerosis 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.

FTMH
Very frequent (80-99%)HP:0031152
Hyperautofluorescent macular lesion
Very frequent (80-99%)HP:0030631
Decreased visual acuity
Frequent (30-79%)HP:0007663
Foveal photoreceptor outer segment loss on macular OCT
Frequent (30-79%)HP:0030615
Hypopigmentation of the fundus
Frequent (30-79%)HP:0007894
Macular atrophy
Frequent (30-79%)HP:0007401
Poor vision
Frequent (30-79%)HP:0000505
Subacute deterioration of visual acuity
Frequent (30-79%)HP:0007924
Visual loss
Frequent (30-79%)HP:0000572
Absent retinal pigment epithelium
Occasional (5-29%)HP:0007980
Choriocapillaris atrophy
Occasional (5-29%)HP:0030491
Chorioretinal atrophy
Occasional (5-29%)HP:0000533
Drusen
Occasional (5-29%)HP:0011510
Perifoveal ring of hyperautofluorescence
Occasional (5-29%)HP:0030629
RPE irregularity
Occasional (5-29%)HP:0007814
Difficulties with night vision
Very rare (1-4%)HP:0000662
Dyschromatopsia
Very rare (1-4%)HP:0007641
Pigmentary retinal deposits
HP:0000580

Quick Facts

SNOMED CT
231996009
UMLS CUI
C1536451
Fully Specified Name
Central areolar choroidal sclerosis (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
18
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.