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RGD DISEASE ONTOLOGY - ANNOTATIONS

RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) 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:Meesmann corneal dystrophy
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Accession:DOID:0060451 term browser browse the term
Definition:An epithelial and subepithelial dystrophy that is characterized by the formation of tiny round cysts in the corneal epithelium. (DO)
Synonyms:exact_synonym: Juvenile Hereditary Epithelial Dystrophy;   MECD;   Meesman's corneal dystrophy;   Meesmann corneal dystrophies;   Meesmann corneal epithelial dystrophy;   Stocker-Holt dystrophy;   juvenile epithelial corneal dystrophy of Meesmann
 primary_id: MESH:D053559
 xref: GARD:9688;   ICD10CM:H18.52;   ICD9CM:371.51;   NCI:C84795;   OMIM:PS122100;   ORDO:98954
For additional species annotation, visit the Alliance of Genome Resources.


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Meesmann corneal dystrophy term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G KRT12 keratin 12 EXP CTD Direct Evidence: marker/mechanism CTD NCBI chr17:40,861,303...40,867,223
Ensembl chr17:40,861,303...40,867,223
JBrowse link
Meesmann corneal dystrophy 1 term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G KRT12 keratin 12 IAGP ClinVar Annotator: match by term: Meesmann corneal dystrophy 1 ClinVar
OMIM
PMID:9171831, PMID:9399908, PMID:10644419, PMID:22174841 NCBI chr17:40,861,303...40,867,223
Ensembl chr17:40,861,303...40,867,223
JBrowse link
Meesmann corneal dystrophy 2 term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G KRT3 keratin 3 IAGP ClinVar Annotator: match by term: Meesmann corneal dystrophy 2 OMIM
ClinVar
PMID:9171831, PMID:16227835, PMID:18806880 NCBI chr12:52,789,685...52,805,735
Ensembl chr12:52,789,685...52,796,117
JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 18864
    sensory system disease 5735
      eye disease 3010
        corneal disease 203
          corneal dystrophy 54
            epithelial and subepithelial dystrophy 6
              Meesmann corneal dystrophy 2
                Meesmann corneal dystrophy 1 1
                Meesmann corneal dystrophy 2 1
Path 2
Term Annotations click to browse term
  disease 18864
    disease of anatomical entity 17349
      nervous system disease 13439
        sensory system disease 5735
          eye disease 3010
            Hereditary Eye Diseases 692
              corneal dystrophy 54
                epithelial and subepithelial dystrophy 6
                  Meesmann corneal dystrophy 2
                    Meesmann corneal dystrophy 1 1
                    Meesmann corneal dystrophy 2 1
paths to the root

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