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.
Xeroderma pigmentosum, group B
Childhood type dermatomyositis
Frequent (30-79%)
Bloom syndrome
Frequent (30-79%)
Hereditary coproporphyria
Occasional (5-29%)
Tryptophanuria with dwarfism
Benign lymphocytic infiltration of Jessner
Frequent (30-79%)
Cockayne syndrome
Frequent (30-79%)
Congenital erythropoietic porphyria
Xeroderma pigmentosum, group C
Ring chromosome 21 syndrome
Occasional (5-29%)
Xeroderma pigmentosum, group G
Always present (100%)
Cerebro-oculo-facio-skeletal syndrome
Frequent (30-79%)
Disseminated superficial actinic porokeratosis
Frequent (30-79%)
Xeroderma pigmentosum, group F
Xeroderma pigmentosum, group A
Always present (100%)
Smith-Lemli-Opitz syndrome
Frequent (30-79%)
Xeroderma pigmentosum
Very frequent (80-99%)
Erythropoietic protoporphyria
Very frequent (80-99%)
Actinic reticuloid
Very frequent (80-99%)
Systemic lupus erythematosus
Occasional (5-29%)
Xeroderma pigmentosum, group E
Variegate porphyria
Frequent (30-79%)
Familial porphyria cutanea tarda
Always present (100%)
Porphyria cutanea tarda
Very frequent (80-99%)
Xeroderma pigmentosum, group D
Always present (100%)
Quick Facts
- SNOMED CT
- 90128006
- UMLS CUI
- C0206051
- Fully Specified Name
- Photosensitivity (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.