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Details
Link-It Detail - Human Phenotype - Abnormality of corneal thickness
Debug Stats
  • ### Total Build Time: 19 ms 19.198 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 207 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 206 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=4 ms Completed: 4 ms rowSize= 446 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 780 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.088 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=8 ms Completed: 8 ms rowSize= 14.339 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.026 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of corneal thickness HP:0011486
Definition (1)
An abnormal anteroposterior thickness of the cornea.
Parents (1)
img Abnormality of the cornea HP:0000481
Children (2)
img Decreased corneal thickness HP:0100689
img Increased corneal thickness HP:0011487
Ancestral Roots
RootRoot Plus OneDepthParent
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 (53)

Species:
human : 53
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanKTCN7100887822Keratoconus 7
HumanKTCN8100885803Keratoconus 8
HumanKTCN6100885802Keratoconus 6
HumanKTCN5100885801Keratoconus 5
HumanATOD5117188Dermatitis, atopic, 5
HumanATOD3117187Dermatitis, atopic, 3
HumanATOD6114477Dermatitis, atopic, 6
HumanWBSCR22114049Williams Beuren syndrome chromosome region 22
HumanZNF46984627zinc finger protein 469
HumanANTXR184168anthrax toxin receptor 1
img HP RolledUp, OMIM ID: 230740
HumanSLC2A1081031solute carrier family 2 (facilitated glucose transporter), member 10
img HP RolledUp, OMIM ID: 208050
HumanGNPTAB79158N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits
HumanFKRP79147fukutin related protein
HumanATOD64069Dermatitis, atopic
HumanRPGRIP157096retinitis pigmentosa GTPase regulator interacting protein 1
img HP RolledUp, OMIM ID: 613826
HumanPOMGNT155624protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)
HumanMLXIPL51085MLX interacting protein-like
HumanVSX130813visual system homeobox 1
HumanPOMT229954protein-O-mannosyltransferase 2
HumanTINF226277TERF1 (TRF1)-interacting nuclear factor 2
HumanKIAA127926128KIAA1279
HumanAIPL123746aryl hydrocarbon receptor interacting protein-like 1
HumanCRB123418crumbs homolog 1 (Drosophila)
img HP RolledUp, OMIM ID: 613835
HumanPRDM511107PR domain containing 5
HumanPOMT110585protein-O-mannosyltransferase 1
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0011486Abnormality of corneal thickness0self