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Details
Link-It Detail - Disease - Hypodontia
Debug Stats
  • ### Total Build Time: 58 ms 26.509 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 318 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=4 ms Completed: 4 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 7 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 15 bytes
  • CONCEPT_RELATIONSHIPS gt=2 ms Completed: 2 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=49 ms Completed: 49 ms rowSize= 24.880 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.145 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Hypodontia C0020608
Genes (55)

Species:
human : 55
Page Size
Current 25
  Page 1 of 3
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanBBS12166379Bardet-Biedl syndrome 12
img OMIM, Score=1000, UMLKSK CUI: C0020608
HumanEVC2132884Ellis van Creveld syndrome 2
img OMIM, Score=1000, UMLKSK CUI: C0020608
HumanBBS5129880Bardet-Biedl syndrome 5
img OMIM, Score=1000, UMLKSK CUI: C0020608
HumanEDARADD128178EDAR-associated death domain
img OMIM, Score=1000, UMLKSK CUI: C0020608
HumanTTC8123016tetratricopeptide repeat domain 8
img OMIM, Score=1000, UMLKSK CUI: C0020608
HumanTMEM6791147transmembrane protein 67
img OMIM, Score=1000, UMLKSK CUI: C0020608
HumanARL684100ADP-ribosylation factor-like 6
img OMIM, Score=1000, UMLKSK CUI: C0020608
HumanWNT10A80326wingless-type MMTV integration site family, member 10A
img OMIM, Score=833, UMLKSK CUI: C0020608
HumanCEP29080184centrosomal protein 290kDa
img OMIM, Score=1000, UMLKSK CUI: C0020608
HumanBBS1079738Bardet-Biedl syndrome 10
img OMIM, Score=1000, UMLKSK CUI: C0020608
HumanPORCN64840porcupine homolog (Drosophila)
img OMIM, Score=1000, UMLKSK CUI: C0020608
img OMIM, Score=1000, UMLKSK CUI: C0020608
HumanBBS755212Bardet-Biedl syndrome 7
img OMIM, Score=1000, UMLKSK CUI: C0020608
HumanMKS154903Meckel syndrome, type 1
img OMIM, Score=1000, UMLKSK CUI: C0020608
HumanBCOR54880BCL6 corepressor
img OMIM, Score=1000, UMLKSK CUI: C0020608
HumanBBS927241Bardet-Biedl syndrome 9
img OMIM, Score=1000, UMLKSK CUI: C0020608
HumanTRIM3222954tripartite motif containing 32
img OMIM, Score=1000, UMLKSK CUI: C0020608
HumanEDAR10913ectodysplasin A receptor
img OMIM, Score=1000, UMLKSK CUI: C0020608
HumanGTF2IRD19569GTF2I repeat domain containing 1
img OMIM, Score=1000, UMLKSK CUI: C0020608
HumanADAMTS29509ADAM metallopeptidase with thrombospondin type 1 motif, 2
img OMIM, Score=1000, UMLKSK CUI: C0020608
HumanCLDN19076claudin 1
img OMIM, Score=1000, UMLKSK CUI: C0020608
img OMIM, Score=1000, UMLKSK CUI: C0020608
HumanTP638626tumor protein p63
img OMIM, Score=1000, UMLKSK CUI: C0020608
img OMIM, Score=1000, UMLKSK CUI: C0020608
HumanIKBKG8517inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma
img OMIM, Score=1000, UMLKSK CUI: C0020608
HumanAXIN28313axin 2
img GENERIF, Score=1000, Pubmed Id: 15042511, UMLKSK CUI: C0020608
HumanMKKS8195McKusick-Kaufman syndrome
img OMIM, Score=1000, UMLKSK CUI: C0020608
HumanWHSC17468Wolf-Hirschhorn syndrome candidate 1
img OMIM, Score=1000, UMLKSK CUI: C0020608
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0020608Hypodontia0self