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Details
Link-It Detail - Disease - Enophthalmos
Debug Stats
  • ### Total Build Time: 39 ms 13.599 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 322 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 194 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= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=4 ms Completed: 4 ms rowSize= 552 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=4 ms Completed: 4 ms rowSize= 1.492 KB
  • CONCEPT_RELATIONSHIPS gt=22 ms Completed: 22 ms rowSize= 7.571 KB
  • CONCEPT_GENES gt=3 ms Completed: 3 ms rowSize= 2.127 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.146 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Enophthalmos C0014306
Definition (1)
Recession of the eyeball into the orbit.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Orbital Diseases C0029182
Ancestral Roots
RootRoot Plus OneDepthParent
img Eye Diseases C0015397img Orbital Diseases C00291823img Orbital Diseases C0029182
Relationships (17)

Relation Types:
diso_​to_​anat : 4
diso_​to_​diso : 13


Relationships:
none : 9
classifies : 1
expanded_​form_​of : 1
isa : 4
mapped_​to : 2
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO27img Orbital Fractures C0029184
DISO_to_ANAT22img Maxillary Sinus C0024957
DISO_to_ANAT22img Ocular orbit C0029180
DISO_to_DISO20img 2-01 DISEASES OF THE NASAL SINUSES C0030469
DISO_to_ANAT17img Maxillary Sinus C0024957
DISO_to_DISO17img Orbital Fractures C0029184
DISO_to_DISO16img 2-01 DISEASES OF THE NASAL SINUSES C0030469
DISO_to_ANAT15img Ocular orbit C0029180
DISO_to_DISO12img Maxillary Sinusitis C0024959
DISO_to_DISOisaimg Enophth d/t orbit atrphy C0155281
DISO_to_DISOisaimg Enophthalmia secondary to temporalis muscle atrophy C0521750
DISO_to_DISOexpanded_form_ofimg Enophthalmos C0014306
DISO_to_DISOisaimg Enophthalmos due to surgery C0271340
DISO_to_DISOisaimg Enophthalmos due to trauma C0339146
DISO_to_DISOmapped_toimg Enophthalmos present C0578597
DISO_to_DISOmapped_toimg O/E - enophthalmos present C0347835
DISO_to_DISOclassifiesimg Other disease of eye C0497217
Genes (2)

Species:
human : 2
SpeciesGeneGeneIdGene NameEvidence
HumanNDP4693Norrie disease (pseudoglioma)
img OMIM, Score=1000, UMLKSK CUI: C0014306
HumanFBN12200fibrillin 1
img OMIM, Score=1000, UMLKSK CUI: C0014306
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0014306Enophthalmos0self