Term Name: gelatinous drop-like corneal dystrophy
Synonyms: corneal amyloidosis, GDCD, primary familial amyloidosis of the cornea, subepithelial amyloidosis of the cornea
Definition: An epithelial and subepithelial dystrophy that is characterized by severe corneal amyloidosis leading to blindness and that has_material_basis_in homozygous or compound heterozygous mutation in the TACSTD2 gene which encodes the monoclonal antibody-defined, tumor-associated antigen GA733-1, on chromosome 1p32.
Ontology: Human Disease [DOID:0060449]   ( DOID:0060449 )

Relationships
is a type of: autosomal recessive disease epithelial and subepithelial dystrophy