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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:Eales Disease
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Accession:DOID:9004932 term browser browse the term
Synonyms:exact_synonym: Idiopathic obliterative vasculopathy;   Idiopathic recurrent vitreal hemorrhage
 primary_id: MESH:C538011;   RDO:0003941
For additional species annotation, visit the Alliance of Genome Resources.


show annotations for term's descendants           Sort by:
 
Eales Disease term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G HLA-B major histocompatibility complex, class I, B IAGP DNA:polymorphisms, haplotypes:cds:HLA-B12, HLA-B44 (human) RGD PMID:9756436 RGD:7365108 NCBI chr 6:31,353,875...31,357,179
Ensembl chr 6:31,269,491...31,357,188
JBrowse link
G IL10 interleukin 10 IAGP DNA:SNP, haplotype:promoter RGD PMID:20720222 RGD:7364860 NCBI chr 1:206,767,602...206,772,494
Ensembl chr 1:206,767,602...206,774,541
JBrowse link
G IL1B interleukin 1 beta IEP RGD PMID:19585364 RGD:7401211 NCBI chr 2:112,829,751...112,836,843
Ensembl chr 2:112,829,751...112,836,816
JBrowse link
G IL6 interleukin 6 susceptibility IEP
IAGP
protein:increased expression:serum:
DNA:polymorphism:promoter:-174G>C(human)
RGD PMID:22025890, PMID:22025890 RGD:7829790, RGD:7829790 NCBI chr 7:22,725,889...22,732,002
Ensembl chr 7:22,725,884...22,732,002
JBrowse link
G TNF tumor necrosis factor disease_progression
severity
IAGP
IEP
DNA:SNP, haplotype:promoter
protein:increased expression:serum:
protein:increased expression:vitreous fluid:
RGD PMID:20720222, PMID:19585364, PMID:21849807, PMID:21394064, PMID:21139707 RGD:7364860, RGD:7401211, RGD:7394772, RGD:7387275, RGD:7387277 NCBI chr 6:31,575,565...31,578,336
Ensembl chr 6:31,575,565...31,578,336
JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 18837
    sensory system disease 5717
      eye disease 2994
        retinal disease 983
          retinal vasculitis 7
            Eales Disease 5
Path 2
Term Annotations click to browse term
  disease 18837
    disease of anatomical entity 17323
      nervous system disease 13417
        sensory system disease 5717
          eye disease 2994
            retinal disease 983
              retinal vascular disease 168
                retinal vasculitis 7
                  Eales Disease 5
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.