Gelatinous drop-like corneal dystrophy
Also known as GDCD, corneal amyloidosis, primary familial amyloidosis of the cornea, subepithelial amyloidosis of the cornea+10 more
GDCD, corneal amyloidosis, primary familial amyloidosis of the cornea, subepithelial amyloidosis of the cornea, CDGDL, Cdgdl, GDLD, amyloid corneal dystrophy, Japanese type, amyloidosis corneal, amyloidosis, corneal, corneal dystrophy, gelatinous drop-like, corneal dystrophy, lattice type 3, lattice corneal dystrophy type 3, lattice corneal dystrophy, type 3.
What's happening now
An analyst briefing on current research, clinical, regulatory and industry activity surrounding this disease.
Associated genes
Genes associated with this disease in the canonical knowledge graph (Open Targets evidence). Number shows the association score.
Disease biology
Proteins whose encoding gene is associated with this disease, reached through the canonical gene→disease graph. Number shows the gene's association score.
Reference
Authoritative identity, definition & identifiers.
GDCD, corneal amyloidosis, primary familial amyloidosis of the cornea, subepithelial amyloidosis of the cornea, CDGDL, Cdgdl, GDLD, amyloid corneal dystrophy, Japanese type, amyloidosis corneal, amyloidosis, corneal, corneal dystrophy, gelatinous drop-like, corneal dystrophy, lattice type 3, lattice corneal dystrophy type 3, lattice corneal dystrophy, type 3
- Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
- Related entities are derived from literature co-mention (studied together) — associative, not causal.