Paralytic lagophthalmos
diseaseOn this page
Also known as paralytic lagophthalmos (disease)
Summary
Paralytic lagophthalmos (MONDO:0001603) is a disease and 4 clinical trials. A subtype of lagophthalmos — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- Clinical trials: 4
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | paralytic lagophthalmos |
| Mondo ID | MONDO:0001603 |
| DOID | DOID:12958 |
| ICD-10-CM | H02.23 |
| ICD-11 | 2122617367 |
| UMLS | C0155197 |
| MedGen | 509844 |
| Is cancer (heuristic) | no |
Also known as: paralytic lagophthalmos · paralytic lagophthalmos (disease)
Data availability: 1 HPO phenotype.
Disease family
This is a subtype of lagophthalmos. 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 adnexa disorder › eyelid disorder › lagophthalmos › paralytic lagophthalmos
Related subtypes (2): mechanical lagophthalmos, cicatricial lagophthalmos
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: 4.
Phase distribution (across all retrieved trials)
| Phase | Trials |
|---|---|
| Not specified | 3 |
| EARLY_PHASE1 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT06895902 | EARLY_PHASE1 | RECRUITING | Suture Lid Spring for Lid Closure in Patients With Facial Nerve Palsy |
| NCT06291818 | Not specified | RECRUITING | Self-Adhering Magnetic Device to Treat Corneal Exposure |
| NCT03848260 | Not specified | SUSPENDED | A Real-Time Magnetic Device Prototype for Temporary Management of Paralytic Lagophthalmos |
| NCT04944498 | Not specified | COMPLETED | Modified Tarsorrhaphy vs Gold Weight Implant for Paralytic Lagophthalmos in Leprosy Patients |
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.