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Details
Link-It Detail - Disease - Fuchs Endothelial Dystrophy
Debug Stats
  • ### Total Build Time: 26 ms 19.345 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 352 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 340 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= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=6 ms Completed: 6 ms rowSize= 567 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=10 ms Completed: 10 ms rowSize= 4.118 KB
  • CONCEPT_RELATIONSHIPS gt=3 ms Completed: 3 ms rowSize= 8.877 KB
  • CONCEPT_GENES gt=3 ms Completed: 3 ms rowSize= 3.740 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.161 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Fuchs Endothelial Dystrophy C0016781
Definition (1)
disorder caused by loss of endothelium of the central cornea; it is characterized by hyaline endothelial outgrowths on Descemet's membrane, epithelial blisters, reduced vision, and pain.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Corneal Dystrophies, Hereditary C0010035
Ancestral Roots
RootRoot Plus OneDepthParent
img Eye Diseases C0015397img Corneal Diseases C00100344img Corneal Dystrophies, Hereditary C0010035
img Eye Diseases C0015397img Eye Diseases, Hereditary C00153984img Corneal Dystrophies, Hereditary C0010035
img Congenital, Hereditary, and Neonatal Diseases and Abnormalities C0027612img Genetic Diseases, Inborn C09501235img Corneal Dystrophies, Hereditary C0010035
Relationships (20)

Relation Types:
diso_​to_​anat : 6
diso_​to_​diso : 10
diso_​to_​phen : 2
diso_​to_​phys : 2


Relationships:
none : 13
is_​associated_​anatomic_​site_​of : 2
mapped_​to : 4
permuted_​term_​of : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANAT59img Corneal Endothelium C0014259
DISO_to_ANAT37img Descemet Membrane C0011665
DISO_to_ANAT32img Cornea C0010031
DISO_to_PHEN27img genetic aspects C0017399
DISO_to_DISO23img Corneal Edema C0010037
DISO_to_DISO22img Complication Aspects C1171258
DISO_to_DISO19img COMPL POSTOP C0032787
DISO_to_ANAT17img Corneal Endothelium C0014259
DISO_to_DISO16img Cornea conical C0022578
DISO_to_DISO14img Complication Aspects C1171258
DISO_to_PHEN14img genetic aspects C0017399
DISO_to_PHYS11img Graft Rejection C0018129
DISO_to_PHYS10img Visual Acuity C0042812
DISO_to_ANATis_associated_anatomic_site_ofimg Cornea C0010031
DISO_to_ANATis_associated_anatomic_site_ofimg Eye C0015392
DISO_to_DISOmapped_toimg CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 2 C1857800
DISO_to_DISOmapped_toimg CORNEAL ENDOTHELIAL DYSTROPHY 2 C1857569
DISO_to_DISOmapped_toimg Cornea guttata with anterior polar cataract C1852558
DISO_to_DISOmapped_toimg Corneal dystrophy, Fuchs' endothelial, 1 C1850959
DISO_to_DISOpermuted_term_ofimg Fuchs Endothelial Dystrophy C0016781
Genes (3)

Species:
human : 3
SpeciesGeneGeneIdGene NameEvidence
HumanTP537157tumor protein p53
img GENERIF, Score=1000, Pubmed Id: 18498065, UMLKSK CUI: C0016781
HumanPITX25308paired-like homeodomain 2
img GENERIF, Score=1000, Pubmed Id: 16876867, UMLKSK CUI: C0016781
HumanCLU1191clusterin
img GENERIF, Score=1000, Pubmed Id: 18378577, UMLKSK CUI: C0016781
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0016781Fuchs Endothelial Dystrophy0self