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Details
Link-It Detail - Disease - RETINAL NONATTACHMENT, NONSYNDROMIC CONGENITAL
Debug Stats
  • ### Total Build Time: 26 ms 9.404 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 390 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_DEFINITION gt=NONE 0 Completed: 0 ms rowSize= 0 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=0 Completed: 0 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=19 ms Completed: 19 ms rowSize= 5.077 KB
  • CONCEPT_GENES gt=4 ms Completed: 4 ms rowSize= 2.696 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.180 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
RETINAL NONATTACHMENT, NONSYNDROMIC CONGENITAL C1857299
Relationships (11)

Relation Types:
diso_​to_​diso : 11


Relationships:
expanded_​form_​of : 1
manifestation_​of : 10
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISOmanifestation_ofimg Absent or greatly attenuated optic nerves and chiasm C3278083
DISO_to_DISOmanifestation_ofimg Bilateral total insensitivity to light C3278079
DISO_to_DISOmanifestation_ofimg Caused by a 6.5kb deletion -21.7kb from the homolog of the drosophila atonal 7 gene (ATOH7, 609875.0001) C3278084
DISO_to_DISOmanifestation_ofimg Esotropia C0014877
DISO_to_DISOmanifestation_ofimg LEUKOCORIA C0152458
DISO_to_DISOmanifestation_ofimg Nystagmus, continuous pendular C3278080
DISO_to_DISOmanifestation_ofimg Phthisis bulbi C0271007
DISO_to_DISOexpanded_form_ofimg RETINAL NONATTACHMENT, NONSYNDROMIC CONGENITAL C1857299
DISO_to_DISOmanifestation_ofimg Retinal nonattachment, congenital C3278082
DISO_to_DISOmanifestation_ofimg Retrolental mass, large C3278081
DISO_to_DISOmanifestation_ofimg Shallow anterior chamber C0860573
Genes (2)

Species:
human : 2
SpeciesGeneGeneIdGene NameEvidence
HumanEGOT100126791eosinophil granule ontogeny transcript (non-protein coding)
img GENERIF, Score=660, Pubmed Id: 17351112, UMLKSK CUI: C1857299
HumanIGF2R3482insulin-like growth factor 2 receptor
img GENERIF, Score=694, Pubmed Id: 18789384, UMLKSK CUI: C1857299
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C1857299RETINAL NONATTACHMENT, NONSYNDROMIC CONGENITAL0self