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Details
Link-It Detail - Human Phenotype - Abnormality of corneal epithelium
Debug Stats
  • ### Total Build Time: 30 ms 28.285 KB
  • CONCEPT_NAME gt=8 ms Completed: 8 ms rowSize= 208 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 276 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=3 ms Completed: 3 ms rowSize= 446 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 1.378 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=2 ms Completed: 2 ms rowSize= 2.088 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=12 ms Completed: 12 ms rowSize= 22.739 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.027 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of corneal epithelium HP:0011495
Definition (1)
Abnormality of the `corneal epithelium` (FMA:58263), that is of the epithelial tissue that covers the front of the cornea.
Parents (1)
img Abnormality of the cornea HP:0000481
Children (4)
img Herpetiform corneal ulceration HP:0007812
img Corneal erosions HP:0200020
img Corneal vascularization HP:0011496
img Keratitis HP:0000491
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
HumanGNPTAB79158N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits
img HP RolledUp, OMIM ID: 252500
HumanSLC39A455630solute carrier family 39 (zinc transporter), member 4
img HP RolledUp, OMIM ID: 201100
HumanMBTPS251360membrane-bound transcription factor peptidase, site 2
img HP RolledUp, OMIM ID: 308800
HumanVSX130813visual system homeobox 1
img HP RolledUp, OMIM ID: 122000
HumanKIAA127926128KIAA1279
img HP RolledUp, OMIM ID: 609460
HumanSPINT210653serine peptidase inhibitor, Kunitz type, 2
img HP RolledUp, OMIM ID: 270420
HumanIKBKAP8518inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase complex-associated protein
img HP RolledUp, OMIM ID: 223900
HumanIKBKG8517inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma
img HP RolledUp, OMIM ID: 308300
HumanXPC7508xeroderma pigmentosum, complementation group C
img HP RolledUp, OMIM ID: 278720
HumanXPA7507xeroderma pigmentosum, complementation group A
img HP RolledUp, OMIM ID: 278700
HumanWT17490Wilms tumor 1
img HP RolledUp, OMIM ID: 106210
HumanTNXB7148tenascin XB
img HP RolledUp, OMIM ID: 130020
HumanTHM7063thymoma
img HP RolledUp, OMIM ID: 274230
HumanTGFBI7045transforming growth factor, beta-induced, 68kDa
img HP RolledUp, OMIM ID: 608470
img HP RolledUp, OMIM ID: 608471
img HP RolledUp, OMIM ID: 602082
HumanTAT6898tyrosine aminotransferase
img HP RolledUp, OMIM ID: 276600
HumanSAT16303spermidine/spermine N1-acetyltransferase 1
img HP RolledUp, OMIM ID: 308800
HumanPOLH5429polymerase (DNA directed), eta
img HP RolledUp, OMIM ID: 278750
HumanPLEC5339plectin
img HP RolledUp, OMIM ID: 226670
HumanPLCG25336phospholipase C, gamma 2 (phosphatidylinositol-specific)
img HP RolledUp, OMIM ID: 614878
HumanPAX65080paired box 6
img HP RolledUp, OMIM ID: 106210
img HP RolledUp, OMIM ID: 148190
HumanNTRK14914neurotrophic tyrosine kinase, receptor, type 1
img HP RolledUp, OMIM ID: 256800
HumanMPV174358MpV17 mitochondrial inner membrane protein
HumanMMP14312matrix metallopeptidase 1 (interstitial collagenase)
img HP RolledUp, OMIM ID: 226600
HumanCHST64166carbohydrate (N-acetylglucosamine 6-O) sulfotransferase 6
HumanLBR3930lamin B receptor
img HP RolledUp, OMIM ID: 613471
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0011495Abnormality of corneal epithelium0self