Retinal cancer
diseaseOn this page
Also known as cancer of retinamalignant neoplasm of retinamalignant neoplasm of the retinamalignant retina neoplasmmalignant retina tumormalignant retina tumourmalignant retinal neoplasmmalignant retinal tumormalignant retinal tumourmalignant tumor of retinamalignant tumor of the retinamalignant tumour of retinamalignant tumour of the retinaretina cancerretinal tumorretinal tumour
Summary
Retinal cancer (MONDO:0003072) is a cancer. A subtype of ocular cancer — 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 | retinal cancer |
| Mondo ID | MONDO:0003072 |
| EFO | EFO:0005716 |
| MeSH | D019572 |
| DOID | DOID:4645 |
| ICD-10-CM | C69.2 |
| ICD-11 | 1758820365 |
| NCIT | C3216 |
| SNOMED CT | 363465007 |
| UMLS | C0024622 |
| MedGen | 6192 |
| Anatomy (UBERON) | UBERON:0000966 |
| Is cancer (heuristic) | yes |
Also known as: cancer of retina · malignant neoplasm of retina · malignant neoplasm of the retina · malignant retina neoplasm · malignant retina tumor · malignant retina tumour · malignant retinal neoplasm · malignant retinal tumor · malignant retinal tumour · malignant tumor of retina · malignant tumor of the retina · malignant tumour of retina · malignant tumour of the retina · retina cancer · retinal tumor · retinal tumour
Disease family
This is a subtype of ocular cancer. 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 etiologic mechanism › cancer or benign tumor › neoplastic disease or syndrome › neoplasm › cancer › nervous system cancer › sensory system cancer › ocular cancer › retinal cancer
Related subtypes (9): lacrimal system cancer, eye carcinoma, uveal cancer, conjunctival cancer, cornea cancer, eye lymphoma, ocular melanoma, eyelid cancer, metastatic malignant neoplasm in the eye
Subtypes (3): retinal cell cancer, retina lymphoma, retinal melanoma
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.