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ONTOLOGY REPORT - ANNOTATIONS


Term:Cogan syndrome
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Accession:DOID:0060216 term browser browse the term
Definition:A condition consisting of inflammatory eye disease usually presenting as interstitial KERATITIS, vestibuloauditory dysfunction, and large- to medium-vessel vasculitis.
Synonyms:exact_synonym: Cogan's Syndrome;   Cogans Syndrome
 related_synonym: diffuse interstitual keratitis
 primary_id: MESH:D055952
 alt_id: RDO:0000612
 xref: GARD:1421;   ORDO:1467
For additional species annotation, visit the Alliance of Genome Resources.


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epithelial basement membrane dystrophy term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Tgfbi transforming growth factor, beta induced JBrowse link 17 8,400,123 8,429,338 RGD:7240710
RGD:8554872
Oculomotor Apraxia, Cogan Type term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Atm ATM serine/threonine kinase JBrowse link 8 58,015,938 58,119,973 RGD:8554872
G Tgm6 transglutaminase 6 JBrowse link 3 122,644,183 122,680,054 RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14759
    syndrome 4210
      Cogan syndrome 3
        Oculomotor Apraxia, Cogan Type 2
        epithelial basement membrane dystrophy 1
Path 2
Term Annotations click to browse term
  disease 14759
    disease of anatomical entity 13978
      nervous system disease 9097
        sensory system disease 4231
          Otorhinolaryngologic Diseases 1035
            auditory system disease 660
              retrocochlear disease 26
                vestibulocochlear nerve disease 19
                  Cogan syndrome 3
                    Oculomotor Apraxia, Cogan Type 2
                    epithelial basement membrane dystrophy 1
paths to the root