Overview
Central scotoma is a finding that may indicate an underlying health condition requiring clinical evaluation.
Associated Conditions
Conditions associated with this symptom based on HPO disease-phenotype annotations.
Fundus flavimaculatus
Very frequent (80-99%)
Achromatopsia
Frequent (30-79%)
Leber's optic atrophy
Frequent (30-79%)
Stargardt's disease
Very frequent (80-99%)
Glaucoma of childhood
Very rare (1-4%)
Hereditary sensory and motor neuropathy, type VI
North Carolina macular dystrophy
Bietti's crystalline retinopathy
Occasional (5-29%)
Acute zonal occult outer retinopathy
Occasional (5-29%)
Carcinoma-associated retinopathy
Occasional (5-29%)
Deafness-dystonia syndrome
Occasional (5-29%)
Autosomal dominant optic atrophy plus syndrome
Always present (100%)
Retinitis punctata albescens
Frequent (30-79%)
Bothnia retinal dystrophy
Occasional (5-29%)
Autosomal dominant optic atrophy classic form
Occasional (5-29%)
Autosomal dominant optic atrophy and cataract
Frequent (30-79%)
Early-onset X-linked optic atrophy
Frequent (30-79%)
Autosomal recessive spastic paraplegia type 55
Always present (100%)
Retinal macular dystrophy type 2
Neurocutaneous melanosis
Occasional (5-29%)
Optic atrophy, ataxia, peripheral neuropathy, global developmental delay syndrome
Occasional (5-29%)
Quick Facts
- SNOMED CT
- 38950008
- UMLS CUI
- C0152191
- Fully Specified Name
- Central scotoma (finding)
- Associated Conditions
- 21
- Diagnostic Tests
- 0
This information is for educational purposes only. If you are experiencing symptoms, please consult a healthcare provider for proper evaluation and diagnosis.