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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:Central Serous Chorioretinopathy
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Accession:DOID:9003248 term browser browse the term
Definition:A visual impairment characterized by the accumulation of fluid under the retina through a defect in the retinal pigment epithelium.
Synonyms:exact_synonym: Central Serous Chorioretinopathies;   Central Serous Retinopathies;   Central Serous Retinopathy
 narrow_synonym: chronic central serous chorioretinopathy;   type II central serous retinopathy
 primary_id: MESH:D056833;   RDO:0007763
 xref: EFO:0009363;   EFO:0009784


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Central Serous Chorioretinopathy term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Serpine1 serpin family E member 1 ISO protein:increased expression:plasma (human)
protein:increased expression:serum (human) 		RGD PMID:10218712 PMID:24446892 RGD:8547738, RGD:8547804 NCBI chr12:25,237,977...25,248,356
Ensembl chr12:19,601,272...19,611,657 		JBrowse link
Term paths to the root
Path 1
Term Annotations click to browse term
  disease 19143
    sensory system disease 7373
      eye disease 3730
        retinal disease 1461
          Central Serous Chorioretinopathy 1
Path 2
Term Annotations click to browse term
  disease 19143
    disease of anatomical entity 18456
      nervous system disease 14362
        Neurologic Manifestations 10461
          sensory system disease 7373
            eye disease 3730
              retinal disease 1461
                Central Serous Chorioretinopathy 1
paths to the root