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Details
Link-It Detail - Human Phenotype - Abnormality of the duodenum
Debug Stats
  • ### Total Build Time: 23 ms 27.611 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 202 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 233 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=2 ms Completed: 2 ms rowSize= 455 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 1.364 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=1 ms Completed: 1 ms rowSize= 2.105 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=13 ms Completed: 13 ms rowSize= 22.106 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.021 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the duodenum HP:0002246
Definition (1)
An abnormality of the duodenum, i.e., the first section of the small intestine.
Parents (1)
img Abnormality of the small intestine HP:0002244
Children (4)
img Duodenal ulcer HP:0002588
img Duodenal stenosis HP:0100867
img Duodenal atresia HP:0002247
img Duodenal stenosis HP:0010449
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the small intestine HP:0002244
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of the small intestine HP:0002244
Genes (26)

Species:
human : 26
Page Size
Current 25
  Page 1 of 2
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanRFX6222546regulatory factor X, 6
img HP RolledUp, OMIM ID: 601346
HumanCHST14113189carbohydrate (N-acetylgalactosamine 4-0) sulfotransferase 14
img HP IEA, OMIM ID: 601776
HumanPORCN64840porcupine homolog (Drosophila)
img HP RolledUp, OMIM ID: 305600
HumanSTRA664220stimulated by retinoic acid 6
img HP RolledUp, OMIM ID: 601186
HumanTTC7A57217tetratricopeptide repeat domain 7A
img HP RolledUp, OMIM ID: 243150
HumanCHD755636chromodomain helicase DNA binding protein 7
img HP RolledUp, OMIM ID: 214800
HumanSEMA3E9723sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E
img HP RolledUp, OMIM ID: 214800
HumanCEP579702centrosomal protein 57kDa
img HP RolledUp, OMIM ID: 614114
HumanYWHAE7531tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon polypeptide
img HP RolledUp, OMIM ID: 247200
HumanTKCR7085torticollis, keloids, cryptorchidism and renal dysplasia
img HP RolledUp, OMIM ID: 314300
HumanSHH6469sonic hedgehog
img HP RolledUp, OMIM ID: 147250
HumanSALL16299sal-like 1 (Drosophila)
img HP RolledUp, OMIM ID: 107480
HumanPLG5340plasminogen
img HP RolledUp, OMIM ID: 217090
HumanPLEC5339plectin
img HP RolledUp, OMIM ID: 226730
HumanPFN15216profilin 1
img HP RolledUp, OMIM ID: 247200
HumanPAFAH1B15048platelet-activating factor acetylhydrolase 1b, regulatory subunit 1 (45kDa)
img HP RolledUp, OMIM ID: 247200
HumanMYCN4613v-myc avian myelocytomatosis viral oncogene neuroblastoma derived homolog
img HP RolledUp, OMIM ID: 164280
HumanMTR45485-methyltetrahydrofolate-homocysteine methyltransferase
img HP RolledUp, OMIM ID: 190685
HumanJBS3719Jacobsen syndrome
img HP RolledUp, OMIM ID: 147791
HumanITGB43691integrin, beta 4
img HP RolledUp, OMIM ID: 226730
HumanITGA63655integrin, alpha 6
img HP RolledUp, OMIM ID: 226730
HumanGATA12623GATA binding protein 1 (globin transcription factor 1)
img HP RolledUp, OMIM ID: 190685
HumanFOXF12294forkhead box F1
img HP RolledUp, OMIM ID: 265380
HumanFBN22201fibrillin 2
img HP RolledUp, OMIM ID: 121050
HumanDCR1637Down syndrome chromosome region
img HP RolledUp, OMIM ID: 190685
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0002246Abnormality of the duodenum0self