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RGD uses the Human Disease Ontology (DO, for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.

Term:gelatinous drop-like corneal dystrophy
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Accession:DOID:0060449 term browser browse the term
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. (DO)
Synonyms:exact_synonym: CDGDL;   Corneal amyloidosis;   GDCD;   GDLD;   amyloid corneal dystrophy, Japanese type;   lattice corneal dystrophy type III;   lattice corneal dystrophy type3;   lattice corneal dystrophy, type 3;   primary familial amyloidosis of the cornea;   subepithelial amyloidosis of the cornea
 primary_id: MESH:C535480
 alt_id: OMIM:204870
 xref: NCI:C142805;   ORDO:98957
For additional species annotation, visit the Alliance of Genome Resources.

show annotations for term's descendants           Sort by:
gelatinous drop-like corneal dystrophy term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Clu clusterin ISO RGD PMID:10502582 RGD:8699502 NCBI chr15:42,626,612...42,665,858
Ensembl chr15:42,640,146...42,665,857
JBrowse link
G Tacstd2 tumor-associated calcium signal transducer 2 ISO ClinVar Annotator: match by OMIM:204870
ClinVar Annotator: match by term: Lattice corneal dystrophy Type III
PMID:10192395, PMID:12107443, PMID:15652848, PMID:28492532 NCBI chr 4:98,341,187...98,342,887
Ensembl chr 4:98,341,188...98,342,887
JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16023
    sensory system disease 5231
      eye disease 2664
        corneal disease 189
          corneal dystrophy 44
            epithelial and subepithelial dystrophy 5
              gelatinous drop-like corneal dystrophy 2
Path 2
Term Annotations click to browse term
  disease 16023
    disease of anatomical entity 15278
      nervous system disease 10897
        sensory system disease 5231
          eye disease 2664
            Hereditary Eye Diseases 580
              corneal dystrophy 44
                epithelial-stromal TGFBI dystrophy 5
                  lattice corneal dystrophy 4
                    gelatinous drop-like corneal dystrophy 2
paths to the root


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.