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Details
Link-It Detail - Disease - Hypertensive Retinopathy
Debug Stats
  • ### Total Build Time: 59 ms 14.387 KB
  • CONCEPT_NAME gt=4 ms Completed: 4 ms rowSize= 346 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 209 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 7 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 15 bytes
  • CONCEPT_RELATIONSHIPS gt=35 ms Completed: 35 ms rowSize= 5.836 KB
  • CONCEPT_GENES gt=14 ms Completed: 14 ms rowSize= 6.780 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.158 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Hypertensive Retinopathy C0152132
Definition (1)
Degenerative changes to the RETINA due to HYPERTENSION.
Relationships (11)

Relation Types:
diso_​to_​anat : 2
diso_​to_​diso : 9


Relationships:
none : 3
associated_​with : 1
classifies : 2
clinically_​similar : 2
is_​associated_​anatomic_​site_​of : 2
mapped_​to : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO6img Hypertension C0020538
DISO_to_DISO3img Complication Aspects C1171258
DISO_to_DISO3img Heart Diseases C0018799
DISO_to_ANATis_associated_anatomic_site_ofimg Eye C0015392
DISO_to_ANATis_associated_anatomic_site_ofimg Retina C0035298
DISO_to_DISOclinically_similarimg HYPERTENSIVE RETINOPATHY ACUTE C0519025
DISO_to_DISOclinically_similarimg HYPERTENSIVE RETINOPATHY CHRONIC C0519026
DISO_to_DISOassociated_withimg Hypertension C0020538
DISO_to_DISOmapped_toimg Hypertensive Retinopathy C0152132
DISO_to_DISOclassifiesimg Other retinal disorders C0339438
DISO_to_DISOclassifiesimg Retinal detachments; defects; vascular occlusion; and retinopathy C0809995
Genes (7)

Species:
human : 7
SpeciesGeneGeneIdGene NameEvidence
HumanKIF1B23095kinesin family member 1B
img OMIM, Score=1000, UMLKSK CUI: C0152132
HumanADIPOQ9370adiponectin, C1Q and collagen domain containing
img GENERIF, Score=901, Pubmed Id: 15745931, UMLKSK CUI: C0152132
HumanVHL7428von Hippel-Lindau tumor suppressor, E3 ubiquitin protein ligase
img OMIM, Score=1000, UMLKSK CUI: C0152132
HumanSDHD6392succinate dehydrogenase complex, subunit D, integral membrane protein
img OMIM, Score=1000, UMLKSK CUI: C0152132
HumanSDHB6390succinate dehydrogenase complex, subunit B, iron sulfur (Ip)
img OMIM, Score=1000, UMLKSK CUI: C0152132
HumanRET5979ret proto-oncogene
img OMIM, Score=1000, UMLKSK CUI: C0152132
HumanGDNF2668glial cell derived neurotrophic factor
img OMIM, Score=1000, UMLKSK CUI: C0152132
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0152132Hypertensive Retinopathy0self