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Details
Link-It Detail - Human Phenotype - Abnormality of the curvature of the cornea
Debug Stats
  • ### Total Build Time: 24 ms 29.273 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 217 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=2 ms Completed: 2 ms rowSize= 776 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 1.065 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=2 ms Completed: 2 ms rowSize= 3.946 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=15 ms Completed: 15 ms rowSize= 22.111 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.036 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the curvature of the cornea HP:0100691
Parents (2)
img Abnormality of corneal size HP:0001120
img Abnormality of the cornea HP:0000481
Children (3)
img Congenital cornea plana HP:0007720
img Increased corneal curvature HP:0100692
img Astigmatism HP:0000483
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of corneal size HP:0001120
img All HP:0000001img Phenotypic abnormality HP:00001189img Abnormality of corneal size HP:0001120
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of the cornea HP:0000481
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of the cornea HP:0000481
Genes (73)

Species:
human : 73
Page Size
Current 25
  Page 1 of 3
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanKTCN7100887822Keratoconus 7
img HP RolledUp, OMIM ID: 614629
HumanKTCN8100885803Keratoconus 8
img HP RolledUp, OMIM ID: 614628
HumanKTCN6100885802Keratoconus 6
img HP RolledUp, OMIM ID: 614623
HumanKTCN5100885801Keratoconus 5
img HP RolledUp, OMIM ID: 614622
HumanDEL2Q23.1100820633
img HP RolledUp, OMIM ID: 156200
HumanBED100653365Bornholm eye disease
img HP RolledUp, OMIM ID: 300843
HumanDUP5P13100379202Chromosome 5p13 duplication syndrome
img HP RolledUp, OMIM ID: 613174
HumanNYS5780901Nystagmus 5, infantile periodic alternating
img HP RolledUp, OMIM ID: 300589
HumanMIR184406960microRNA 184
img HP RolledUp, OMIM ID: 614303
HumanKCNV2169522potassium channel, subfamily V, member 2
img HP RolledUp, OMIM ID: 610356
HumanBBS12166379Bardet-Biedl syndrome 12
img HP RolledUp, OMIM ID: 209900
HumanBBS5129880Bardet-Biedl syndrome 5
img HP RolledUp, OMIM ID: 209900
HumanTTC8123016tetratricopeptide repeat domain 8
img HP RolledUp, OMIM ID: 209900
HumanATOD5117188Dermatitis, atopic, 5
img HP RolledUp, OMIM ID: 603165
HumanATOD3117187Dermatitis, atopic, 3
img HP RolledUp, OMIM ID: 603165
HumanATOD6114477Dermatitis, atopic, 6
img HP RolledUp, OMIM ID: 603165
HumanWBSCR22114049Williams Beuren syndrome chromosome region 22
img HP RolledUp, OMIM ID: 194050
HumanTMEM6791147transmembrane protein 67
img HP RolledUp, OMIM ID: 209900
HumanUBE3B89910ubiquitin protein ligase E3B
img HP RolledUp, OMIM ID: 615057
HumanZNF46984627zinc finger protein 469
img HP RolledUp, OMIM ID: 229200
HumanANTXR184168anthrax toxin receptor 1
img HP RolledUp, OMIM ID: 230740
HumanARL684100ADP-ribosylation factor-like 6
img HP RolledUp, OMIM ID: 209900
HumanSLC2A1081031solute carrier family 2 (facilitated glucose transporter), member 10
img HP RolledUp, OMIM ID: 208050
HumanCEP29080184centrosomal protein 290kDa
img HP RolledUp, OMIM ID: 209900
HumanBBS1079738Bardet-Biedl syndrome 10
img HP RolledUp, OMIM ID: 209900
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0100691Abnormality of the curvature of the cornea0self