Conjunctival vascular disorder
diseaseOn this page
Also known as conjunctival vasculature diseaseconjunctival vasculature disease or disorderdisease of conjunctival vasculaturedisease or disorder of conjunctival vasculaturedisorder of conjunctival vasculaturevascular abnormalities of conjunctiva
Summary
Conjunctival vascular disorder (MONDO:0001174) is a disease. A subtype of ocular vascular disorder — 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 | conjunctival vascular disorder |
| Mondo ID | MONDO:0001174 |
| DOID | DOID:10989 |
| ICD-10-CM | H11.41 |
| NCIT | C35116 |
| SNOMED CT | 74100001 |
| UMLS | C0042370 |
| MedGen | 12052 |
| Anatomy (UBERON) | UBERON:0010366 |
| Is cancer (heuristic) | no |
Also known as: conjunctival vascular disorder · conjunctival vasculature disease · conjunctival vasculature disease or disorder · disease of conjunctival vasculature · disease or disorder of conjunctival vasculature · disorder of conjunctival vasculature · vascular abnormalities of conjunctiva
Disease family
Classification path: disease › human disease › disease by body system or component › disorder of orbital region › eye disorder › ocular vascular disorder › conjunctival vascular disorder
Related subtypes (2): optic choroid disorder, retinal vascular disorder
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.