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Details
Link-It Detail - Human Phenotype - Abnormality of the periungual region
Debug Stats
  • ### Total Build Time: 34 ms 17.320 KB
  • CONCEPT_NAME gt=11 ms Completed: 11 ms rowSize= 211 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 223 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=1 ms Completed: 1 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= 1.076 KB
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 1.056 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=4 ms Completed: 4 ms rowSize= 4.865 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=8 ms Completed: 8 ms rowSize= 8.725 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.030 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the periungual region HP:0100803
Definition (1)
An abnormality of the region around the nails of the fingers or toes.
Parents (3)
img Abnormality of the nail HP:0001597
img Regional abnormality of skin HP:0011356
img Abnormality of the skin HP:0000951
Children (3)
img Ungual fibroma HP:0100804
img Circumungual hyperkeratosis HP:0008399
img Paronychia HP:0001818
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of the nail HP:0001597
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the nail HP:0001597
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of the nail HP:0001597
img All HP:0000001img Phenotypic abnormality HP:00001186img Regional abnormality of skin HP:0011356
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of the skin HP:0000951
Genes (13)

Species:
human : 13
SpeciesGeneGeneIdGene NameEvidence
HumanWNK165125WNK lysine deficient protein kinase 1
img HP RolledUp, OMIM ID: 201300
HumanSLC39A455630solute carrier family 39 (zinc transporter), member 4
img HP RolledUp, OMIM ID: 201100
HumanAIP9049aryl hydrocarbon receptor interacting protein
img HP RolledUp, OMIM ID: 219090
HumanIKBKG8517inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma
HumanTSC27249tuberous sclerosis 2
img HP RolledUp, OMIM ID: 606690
HumanTSC17248tuberous sclerosis 1
img HP RolledUp, OMIM ID: 606690
HumanADAM176868ADAM metallopeptidase domain 17
img HP RolledUp, OMIM ID: 614328
HumanSTAT36774signal transducer and activator of transcription 3 (acute-phase response factor)
img HP RolledUp, OMIM ID: 147060
HumanPLEC5339plectin
HumanKRT163868keratin 16
HumanKRT6A3853keratin 6A
HumanGNAS2778GNAS complex locus
img HP RolledUp, OMIM ID: 219090
HumanCTSC1075cathepsin C
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0100803Abnormality of the periungual region0self