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Details
Link-It Detail - Human Phenotype - Abdominal pain
Debug Stats
  • ### Total Build Time: 38 ms 28.167 KB
  • CONCEPT_NAME gt=9 ms Completed: 9 ms rowSize= 189 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 197 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= 767 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 764 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.081 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=19 ms Completed: 19 ms rowSize= 23.061 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.009 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abdominal pain HP:0002027
Definition (1)
Pain perceived to originate in the abdomen.
Parents (2)
img Abnormality of the abdomen HP:0001438
img Abdominal symptom HP:0011458
Children (2)
img Abdominal colic HP:0011848
img Episodic abdominal pain HP:0002574
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001184img Abnormality of the abdomen HP:0001438
img All HP:0000001img Phenotypic abnormality HP:00001185img Abdominal symptom HP:0011458
Genes (129)

Species:
human : 129
Page Size
Current 25
  Page 1 of 6
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanIBD11100529151Inflammatory bowel disease 11
img HP IEA, OMIM ID: 191390
HumanWG474168Wegener granulomatosis
img HP TAS, OMIM ID: 608710
HumanBLOC1S3388552biogenesis of lysosomal organelles complex-1, subunit 3
img HP IEA, OMIM ID: 203300
HumanMMS338340Malignant mesothelioma, susceptibility to
img HP TAS, OMIM ID: 156240
HumanIBD9317669inflammatory bowel disease 9
img HP IEA, OMIM ID: 266600
HumanIBD8170595inflammatory bowel disease 8
img HP IEA, OMIM ID: 266600
HumanIL23R149233interleukin 23 receptor
img HP IEA, OMIM ID: 266600
HumanNLRP3114548NLR family, pyrin domain containing 3
img HP TAS, OMIM ID: 191900
HumanWBSCR22114049Williams Beuren syndrome chromosome region 22
img HP TAS, OMIM ID: 194050
HumanHPS489781Hermansky-Pudlak syndrome 4
img HP IEA, OMIM ID: 203300
HumanLCS184565lymphedema-cholestasis syndrome 1
img HP TAS, OMIM ID: 214900
HumanHPS384343Hermansky-Pudlak syndrome 3
img HP IEA, OMIM ID: 203300
HumanDTNBP184062dystrobrevin binding protein 1
img HP IEA, OMIM ID: 203300
HumanITPKC80271inositol-trisphosphate 3-kinase C
img HP TAS, OMIM ID: 611775
HumanHPS679803Hermansky-Pudlak syndrome 6
img HP IEA, OMIM ID: 203300
HumanPORCN64840porcupine homolog (Drosophila)
img HP TAS, OMIM ID: 305600
HumanABCG864241ATP-binding cassette, sub-family G (WHITE), member 8
img HP IEA, OMIM ID: 210250
HumanABCG564240ATP-binding cassette, sub-family G (WHITE), member 5
img HP IEA, OMIM ID: 210250
HumanNOD264127nucleotide-binding oligomerization domain containing 2
img HP IEA, OMIM ID: 266600
HumanIBD757042inflammatory bowel disease 7
img HP IEA, OMIM ID: 266600
HumanMLXIPL51085MLX interacting protein-like
img HP TAS, OMIM ID: 194050
HumanIBD650942inflammatory bowel disease 6
img HP IEA, OMIM ID: 266600
HumanIBD550941inflammatory bowel disease 5
img HP IEA, OMIM ID: 266600
HumanIBD450608inflammatory bowel disease 4
img HP IEA, OMIM ID: 266600
HumanCD20930835CD209 molecule
img HP TAS, OMIM ID: 614371
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0002027Abdominal pain0self