Photokeratitis

Summary

Photokeratitis (MONDO:0001760) is a disease. A subtype of keratitis — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

Field	Value
Canonical name	photokeratitis
Mondo ID	MONDO:0001760
DOID	DOID:13626
ICD-10-CM	H16.13
ICD-11	1566990302
NCIT	C118750
SNOMED CT	1714005
UMLS	C0155078
MedGen	509774
GARD	0023006
Is cancer (heuristic)	no

Also known as: ultraviolet keratitis

Disease family

This is a subtype of keratitis. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.

Classification path: disease › human disease › disease by body system or component › disorder of orbital region › eye disorder › corneal disorder › keratitis › photokeratitis

Related subtypes (10): macular keratitis, superficial keratitis, scleroperikeratitis, filamentary keratitis, corneal ulcer, keratoconjunctivitis, deep keratitis, corneal neovascularization, autosomal dominant keratitis, corneal infection

Genetics & variants

GWAS landscape

No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.

Variant details and genetic-evidence tiers

No tiered GWAS variants or ClinVar records for this disease.

Genes & proteins

No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).

Function

No pathway enrichment — requires an associated-gene cohort.

Therapeutics

No druggable-target or therapeutic data for this disease’s cohort.

Clinical trials & evidence

Clinical trials

Clinical trials: 0.