Choroid cancer

disease
On this page

Also known as cancer of optic choroidchoroid neoplasmchoroidal tumorchoroidal tumourmalignant choroid neoplasmmalignant choroid tumormalignant choroid tumourmalignant neoplasm of choroidmalignant neoplasm of optic choroidmalignant neoplasm of the choroidmalignant optic choroid neoplasmmalignant tumor of choroidmalignant tumor of the choroidmalignant tumour of choroidmalignant tumour of the choroidoptic choroid cancer

Summary

Choroid cancer (MONDO:0006700) is a cancer and 3 clinical trials. A subtype of vascular cancer — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Classification: Cancer
  • Clinical trials: 3

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical namechoroid cancer
Mondo IDMONDO:0006700
MeSHD002830
DOIDDOID:12759
ICD-10-CMC69.3
NCITC3566
SNOMED CT363466008
UMLSC0153630
MedGen57794
MedDRA10057405
Anatomy (UBERON)UBERON:0001776
Is cancer (heuristic)yes

Also known as: cancer of optic choroid · choroid neoplasm · choroidal tumor · choroidal tumour · malignant choroid neoplasm · malignant choroid tumor · malignant choroid tumour · malignant neoplasm of choroid · malignant neoplasm of optic choroid · malignant neoplasm of the choroid · malignant optic choroid neoplasm · malignant tumor of choroid · malignant tumor of the choroid · malignant tumour of choroid · malignant tumour of the choroid · optic choroid cancer

Disease family

This is a subtype of vascular 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 tumorneoplastic disease or syndromeneoplasmcancercardiovascular cancervascular cancerchoroid cancer

Related subtypes (6): choroid plexus cancer, malignant jugulotympanic paraganglioma, adrenal cortex carcinoma, epithelioid hemangioendothelioma, angiosarcoma, great vessel cancer

Subtypes (1): malignant choroid 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: 3.

Phase distribution (across all retrieved trials)

PhaseTrials
PHASE31
PHASE11
Not specified1

Top trials by phase / activity

NCTPhaseStatusTitle
NCT00000124PHASE3UNKNOWNCollaborative Ocular Melanoma Study (COMS)
NCT02771340PHASE1COMPLETEDStudy Evaluating Single and Repeated Intravitreal Doses of ICON-1 in Patients With Uveal Melanoma
NCT00406120Not specifiedWITHDRAWNValidation of a Molecular Prognostic Test for Eye Melanoma

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.