Lacrimal system cancer

disease
On this page

Also known as cancer of lacrimal apparatuslacrimal apparatus cancerlacrimal system neoplasmlacrimal system neoplasmslacrimal system tumorlacrimal system tumourmalignant lacrimal apparatus neoplasmmalignant neoplasm of lacrimal apparatusneoplasm of lacrimal systemneoplasm of the lacrimal systemtumor of lacrimal systemtumor of the lacrimal systemtumour of lacrimal systemtumour of the lacrimal system

Summary

Lacrimal system cancer (MONDO:0002460) is a cancer. A subtype of lacrimal apparatus disorder — 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

FieldValue
Canonical namelacrimal system cancer
Mondo IDMONDO:0002460
DOIDDOID:292
ICD-11456911769
NCITC5102
SNOMED CT416510003
UMLSC1334361
MedGen272790
Anatomy (UBERON)UBERON:0001750
Is cancer (heuristic)yes

Also known as: cancer of lacrimal apparatus · lacrimal apparatus cancer · lacrimal system neoplasm · lacrimal system neoplasms · lacrimal system tumor · lacrimal system tumour · malignant lacrimal apparatus neoplasm · malignant neoplasm of lacrimal apparatus · neoplasm of lacrimal system · neoplasm of the lacrimal system · tumor of lacrimal system · tumor of the lacrimal system · tumour of lacrimal system · tumour of the lacrimal system

Disease family

This is a subtype of lacrimal apparatus disorder. 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 regioneye adnexa disorderlacrimal apparatus disorderlacrimal system cancer

Related subtypes (16): lacrimal passage granuloma, eversion of lacrimal punctum, stenosis of lacrimal punctum, stenosis of lacrimal passage, excessive tearing, primary lacrimal atrophy, secondary lacrimal atrophy, stenosis of lacrimal sac, acute inflammation of lacrimal passage, chronic inflammation of lacrimal passage, dry eye syndrome, IgG4-related dacryoadenitis and sialadenitis, isolated congenital alacrima, disorder of lacrimal gland, nasolacrimal duct disorder, syndromic lacrimal system disorder

Subtypes (2): lacrimal duct cancer, lacrimal gland cancer

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.

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