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Details
Link-It Detail - Human Phenotype - Abnormality of oral mucosa
Debug Stats
  • ### Total Build Time: 35 ms 22.573 KB
  • CONCEPT_NAME gt=16 ms Completed: 16 ms rowSize= 201 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 199 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= 451 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 1.988 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.166 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=10 ms Completed: 10 ms rowSize= 17.423 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.021 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of oral mucosa HP:0011830
Definition (1)
Abnormality of the `oral mucosa` (FMA:59660).
Parents (1)
img Abnormality of the oral cavity HP:0000163
Children (6)
img Oral leukoplakia HP:0002745
img Stomatitis HP:0010280
img Oral mucusa blisters HP:0200097
img Oral ulcer HP:0000155
img Oral cavity teleangiectasia HP:0000228
img Oral synechia HP:0010285
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of the oral cavity HP:0000163
Genes (53)

Species:
human : 53
Page Size
Current 25
  Page 1 of 3
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanHHT4791087Telangiectasia, hereditary hemorrhagic, type 4
HumanIBD9317669inflammatory bowel disease 9
HumanIBD8170595inflammatory bowel disease 8
HumanIL23R149233interleukin 23 receptor
HumanNLRP3114548NLR family, pyrin domain containing 3
HumanSLC46A1113235solute carrier family 46 (folate transporter), member 1
img HP RolledUp, OMIM ID: 229050
HumanORAI184876ORAI calcium release-activated calcium modulator 1
HumanDKBI80870Dyskeratosis, hereditary benign intraepithelial
img HP RolledUp, OMIM ID: 127600
HumanCTC180169CTS telomere maintenance complex component 1
img HP RolledUp, OMIM ID: 612199
HumanDCLRE1C64421DNA cross-link repair 1C
img HP RolledUp, OMIM ID: 602450
HumanNOD264127nucleotide-binding oligomerization domain containing 2
HumanIBD757042inflammatory bowel disease 7
HumanLMBRD155788LMBR1 domain containing 1
img HP RolledUp, OMIM ID: 277380
HumanNHP255651NHP2 ribonucleoprotein
img HP RolledUp, OMIM ID: 224230
HumanNOP1055505NOP10 ribonucleoprotein
img HP RolledUp, OMIM ID: 224230
HumanIBD650942inflammatory bowel disease 6
HumanIBD550941inflammatory bowel disease 5
HumanIBD450608inflammatory bowel disease 4
HumanIBD330829inflammatory bowel disease 3
HumanTINF226277TERF1 (TRF1)-interacting nuclear factor 2
img HP RolledUp, OMIM ID: 127550
img HP RolledUp, OMIM ID: 268130
img HP RolledUp, OMIM ID: 613990
HumanDLG59231discs, large homolog 5 (Drosophila)
HumanTERT7015telomerase reverse transcriptase
img HP RolledUp, OMIM ID: 127550
HumanTERC7012telomerase RNA component
img HP RolledUp, OMIM ID: 127550
HumanSLC22A46583solute carrier family 22 (organic cation/zwitterion transporter), member 4
HumanNCF44689neutrophil cytosolic factor 4, 40kDa
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0011830Abnormality of oral mucosa0self