Overview
Clinical overview and emergency guidance are pending physician authorship. Graph-derived data (ontology codes, linked conditions, diagnostic biomarkers) is available below.
Associated Conditions
Conditions associated with this symptom based on HPO disease-phenotype annotations.
Juvenile epithelial corneal dystrophy
Fisher's syndrome
Occasional (5-29%)
Dubowitz's syndrome
Occasional (5-29%)
Senter syndrome
Frequent (30-79%)
Hypertyrosinemia, Richner-Hanhart type
Frequent (30-79%)
Bardet-Biedl syndrome
Frequent (30-79%)
Tyrosinase-negative oculocutaneous albinism
Very frequent (80-99%)
Distichiasis-lymphedema syndrome
Very frequent (80-99%)
Hermansky-Pudlak syndrome
Frequent (30-79%)
Fuchs' heterochromic cyclitis
Occasional (5-29%)
Polyglandular autoimmune syndrome, type 1
Frequent (30-79%)
Babesiosis
Occasional (5-29%)
Cockayne syndrome
Occasional (5-29%)
Juvenile nephropathic cystinosis
Frequent (30-79%)
Lyme disease
Occasional (5-29%)
Tonic pupillary reaction
Occasional (5-29%)
Xeroderma pigmentosum, group C
Tyrosinase-positive oculocutaneous albinism
Frequent (30-79%)
Retinitis pigmentosa
Very frequent (80-99%)
Progressive supranuclear ophthalmoplegia
Frequent (30-79%)
Polymorphous corneal dystrophy
Very rare (1-4%)
Hereditary acrodermatitis enteropathica
Frequent (30-79%)
Migraine
Ectrodactyly-ectodermal dysplasia-clefting syndrome
Frequent (30-79%)
Congo-Crimean hemorrhagic fever
Occasional (5-29%)
Quick Facts
- SNOMED CT
- 246622003
- UMLS CUI
- C0085636
- Fully Specified Name
- Eyes sensitive to light (finding)
- Associated Conditions
- 25
- 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.