Benign neoplasm of cornea
disease diseaseOn this page
Also known as benign cornea neoplasmbenign cornea tumorbenign cornea tumourbenign corneal neoplasmbenign corneal tumorbenign corneal tumourbenign neoplasm of the corneabenign tumor of corneabenign tumor of the corneabenign tumour of corneabenign tumour of the corneacornea benign neoplasm
Summary
Benign neoplasm of cornea (MONDO:0021452) is a cancer. A subtype of cornea neoplasm — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- Classification: Cancer
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | benign neoplasm of cornea |
| Mondo ID | MONDO:0021452 |
| ICD-10-CM | D31.1 |
| ICD-11 | 568257604 |
| NCIT | C3623 |
| SNOMED CT | 92070006 |
| UMLS | C0154026 |
| MedGen | 57579 |
| Anatomy (UBERON) | UBERON:0000964 |
| Is cancer (heuristic) | yes |
Also known as: benign cornea neoplasm · benign cornea tumor · benign cornea tumour · benign corneal neoplasm · benign corneal tumor · benign corneal tumour · benign neoplasm of the cornea · benign tumor of cornea · benign tumor of the cornea · benign tumour of cornea · benign tumour of the cornea · cornea benign neoplasm
Disease family
This is a subtype of cornea neoplasm. 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 › cornea neoplasm › benign neoplasm of cornea
Related subtypes (2): corneal intraepithelial neoplasm, cornea cancer
Subtypes (1): pterygium
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.
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.