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Details
Link-It Detail - Human Phenotype - Abnormal tendency to infections of the skin
Debug Stats
  • ### Total Build Time: 27 ms 25.057 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 218 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
  • CONCEPT_NAMESPACE gt=0 Completed: 0 ms rowSize= 168 bytes
  • CONCEPT_PARENTS gt=2 ms Completed: 2 ms rowSize= 444 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 1.048 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=1 ms Completed: 1 ms rowSize= 1.159 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=15 ms Completed: 15 ms rowSize= 20.857 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.037 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormal tendency to infections of the skin HP:0002727
Namespace (1)
medical_genetics
Parents (1)
img Abnormality of the skin HP:0000951
Children (3)
img Erysipelas HP:0001055
img Pyoderma HP:0000999
img Recurrent skin infections HP:0001581
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of the skin HP:0000951
Genes (55)

Species:
human : 55
Page Size
Current 25
  Page 1 of 3
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanNCF1653361neutrophil cytosolic factor 1
img HP RolledUp, OMIM ID: 233700
HumanCCBE1147372collagen and calcium binding EGF domains 1
img HP RolledUp, OMIM ID: 235510
HumanTMC8147138transmembrane channel-like 8
img HP RolledUp, OMIM ID: 226400
HumanATOD5117188Dermatitis, atopic, 5
img HP RolledUp, OMIM ID: 603165
HumanATOD3117187Dermatitis, atopic, 3
img HP RolledUp, OMIM ID: 603165
HumanCANDF1117084candidiasis, familial 1
HumanATOD6114477Dermatitis, atopic, 6
img HP RolledUp, OMIM ID: 603165
HumanCHST14113189carbohydrate (N-acetylgalactosamine 4-0) sulfotransferase 14
img HP RolledUp, OMIM ID: 601776
HumanIL17F112744interleukin 17F
img HP RolledUp, OMIM ID: 613956
HumanLCS184565lymphedema-cholestasis syndrome 1
img HP RolledUp, OMIM ID: 214900
HumanDOCK881704dedicator of cytokinesis 8
img HP RolledUp, OMIM ID: 243700
HumanPORCN64840porcupine homolog (Drosophila)
img HP RolledUp, OMIM ID: 305600
HumanCLEC7A64581C-type lectin domain family 7, member A
img HP RolledUp, OMIM ID: 613108
HumanCARD964170caspase recruitment domain family, member 9
HumanATOD64069Dermatitis, atopic
img HP RolledUp, OMIM ID: 603165
HumanEPG557724ectopic P-granules autophagy protein 5 homolog (C. elegans)
HumanGJC257165gap junction protein, gamma 2, 47kDa
img HP RolledUp, OMIM ID: 613480
HumanPSENEN55851presenilin enhancer 2 homolog (C. elegans)
img HP RolledUp, OMIM ID: 613736
HumanIL17RA23765interleukin 17 receptor A
img HP RolledUp, OMIM ID: 613953
HumanTMC611322transmembrane channel-like 6
img HP RolledUp, OMIM ID: 226400
HumanPSTPIP19051proline-serine-threonine phosphatase interacting protein 1
img HP RolledUp, OMIM ID: 604416
HumanRFXANK8625regulatory factor X-associated ankyrin-containing protein
HumanFCN38547ficolin (collagen/fibrinogen domain containing) 3 (Hakata antigen)
img HP RolledUp, OMIM ID: 613860
HumanIKBKG8517inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma
img HP RolledUp, OMIM ID: 308300
HumanCXCR47852chemokine (C-X-C motif) receptor 4
img HP RolledUp, OMIM ID: 193670
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0002727Abnormal tendency to infections of the skin0self