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Details
Link-It Detail - Disease - Lens Diseases
Debug Stats
  • ### Total Build Time: 173 ms 35.220 KB
  • CONCEPT_NAME gt=9 ms Completed: 9 ms rowSize= 324 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 288 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=2 ms Completed: 2 ms rowSize= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=12 ms Completed: 12 ms rowSize= 548 bytes
  • CONCEPT_CHILDREN gt=12 ms Completed: 12 ms rowSize= 1.373 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.094 KB
  • CONCEPT_RELATIONSHIPS gt=90 ms Completed: 90 ms rowSize= 12.226 KB
  • CONCEPT_GENES gt=40 ms Completed: 40 ms rowSize= 18.036 KB
  • CONCEPT_XREFS gt=7 ms Completed: 7 ms rowSize= 1.147 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Lens Diseases C0023308
Definition (1)
pathologic condition of the transparent biconvex body of the eye situated between the posterior chamber and the vitreous body or lens.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Eye Diseases C0015397
Children (3)
img Lens Subluxation C0023316
img Cataract C0086543
img Aphakia C0003534
Ancestral Roots
RootRoot Plus OneDepthParent
img Eye Diseases C00153972img Eye Diseases C0015397
Relationships (31)

Relation Types:
diso_​to_​anat : 6
diso_​to_​diso : 25


Relationships:
none : 13
is_​associated_​anatomic_​site_​of : 2
isa : 15
permuted_​term_​of : 1
Page Size
Current 25
  Page 1 of 2
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Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANAT47img Lens Capsule, Crystalline C0229232
DISO_to_ANAT40img Lens Capsule, Crystalline C0229232
DISO_to_DISO19img COMPL POSTOP C0032787
DISO_to_DISO17img Complication Aspects C1171258
DISO_to_ANAT16img Lens, Crystalline C0023317
DISO_to_DISO13img Complication Aspects C1171258
DISO_to_DISO13img Disease of Iris C0022078
DISO_to_DISO12img COMPL POSTOP C0032787
DISO_to_DISO12img Exfoliation Syndrome C0206368
DISO_to_ANAT11img Lens, Crystalline C0023317
DISO_to_DISO11img Iris Diseases C0022078
DISO_to_DISO10img COMPL INTRAOP C0021890
DISO_to_DISO10img Nephritis, Hereditary C0027706
DISO_to_ANATis_associated_anatomic_site_ofimg Eye C0015392
DISO_to_ANATis_associated_anatomic_site_ofimg Lens, Crystalline C0023317
DISO_to_DISOisaimg Allergic reaction to lens protein C0271157
DISO_to_DISOisaimg Aphakia C0003534
DISO_to_DISOisaimg Cataract C0086543
DISO_to_DISOisaimg Congenital Lens Disorder C0339350
DISO_to_DISOisaimg Disorder of intraocular lens C0730071
DISO_to_DISOisaimg Disorder of lens capsule C0339372
DISO_to_DISOisaimg Foreign body in lens C0154801
DISO_to_DISOisaimg Injury of lens C0433982
DISO_to_DISOisaimg Irregular astigmatism - lenticular C0339685
DISO_to_DISOpermuted_term_ofimg Lens Diseases C0023308
Genes (140)

Species:
human : 140
Page Size
Current 25
  Page 1 of 6
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanGTF2H5404672general transcription factor IIH, polypeptide 5
INFERRED, Score=800, UMLKSK CUI: C0023308
HumanTMEM114283953transmembrane protein 114
INFERRED, Score=800, UMLKSK CUI: C0023308
HumanBBS12166379Bardet-Biedl syndrome 12
INFERRED, Score=800, UMLKSK CUI: C0023308
HumanESCO2157570establishment of sister chromatid cohesion N-acetyltransferase 2
INFERRED, Score=800, UMLKSK CUI: C0023308
HumanBBS5129880Bardet-Biedl syndrome 5
INFERRED, Score=800, UMLKSK CUI: C0023308
HumanTTC8123016tetratricopeptide repeat domain 8
INFERRED, Score=800, UMLKSK CUI: C0023308
HumanATOD5117188Dermatitis, atopic, 5
INFERRED, Score=800, UMLKSK CUI: C0023308
HumanATOD3117187Dermatitis, atopic, 3
INFERRED, Score=800, UMLKSK CUI: C0023308
HumanATOD6114477Dermatitis, atopic, 6
INFERRED, Score=800, UMLKSK CUI: C0023308
HumanTMEM6791147transmembrane protein 67
INFERRED, Score=800, UMLKSK CUI: C0023308
HumanARL684100ADP-ribosylation factor-like 6
INFERRED, Score=800, UMLKSK CUI: C0023308
HumanADAMTS1081794ADAM metallopeptidase with thrombospondin type 1 motif, 10
INFERRED, Score=800, UMLKSK CUI: C0023308
HumanOPA380207optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia)
INFERRED, Score=800, UMLKSK CUI: C0023308
HumanCEP29080184centrosomal protein 290kDa
INFERRED, Score=800, UMLKSK CUI: C0023308
HumanBBS1079738Bardet-Biedl syndrome 10
INFERRED, Score=800, UMLKSK CUI: C0023308
HumanFKRP79147fukutin related protein
INFERRED, Score=800, UMLKSK CUI: C0023308
HumanPORCN64840porcupine homolog (Drosophila)
INFERRED, Score=800, UMLKSK CUI: C0023308
HumanSALL457167sal-like 4 (Drosophila)
INFERRED, Score=800, UMLKSK CUI: C0023308
HumanC10orf256652chromosome 10 open reading frame 2
INFERRED, Score=800, UMLKSK CUI: C0023308
HumanPEX2655670peroxisomal biogenesis factor 26
INFERRED, Score=800, UMLKSK CUI: C0023308
HumanPOMGNT155624protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)
INFERRED, Score=800, UMLKSK CUI: C0023308
HumanBBS755212Bardet-Biedl syndrome 7
INFERRED, Score=800, UMLKSK CUI: C0023308
HumanMKS154903Meckel syndrome, type 1
INFERRED, Score=800, UMLKSK CUI: C0023308
HumanCNGB354714cyclic nucleotide gated channel beta 3
INFERRED, Score=800, UMLKSK CUI: C0023308
HumanPOMT229954protein-O-mannosyltransferase 2
INFERRED, Score=800, UMLKSK CUI: C0023308
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0023308Lens Diseases0self