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Details
Link-It Detail - Human Phenotype - Abnormality of the gastrointestinal tract
Debug Stats
  • ### Total Build Time: 53 ms 30.363 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 216 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
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  • 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=0 Completed: 0 ms rowSize= 456 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 5.311 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.171 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=47 ms Completed: 47 ms rowSize= 22.046 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.035 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the gastrointestinal tract HP:0011024
Parents (1)
img Abnormality of the abdominal organs HP:0002012
Children (16)
img Gastrointestinal dysmotility HP:0002579
img Abnormality of the esophagus HP:0002031
img Gastrointestinal obstruction HP:0004796
img Peptic ulcer HP:0004398
img Abnormality of the stomach HP:0002577
img Gastrointestinal duplication HP:0011140
img Abnormality of the intestine HP:0002242
img Abnormality of the anus HP:0004378
img Neoplasm of the gastrointestinal tract HP:0007378
img Gastrointestinal inflammation HP:0004386
img Recurrent infection of the gastrointestinal tract HP:0004798
img Gastrointestinal reflux HP:0004793
img Gastrointestinal hemorrhage HP:0002239
img Gastrointestinal atresia HP:0002589
img Gastrointestinal infarctions HP:0005244
img Abnormality of gastrointestinal vasculature HP:0004296
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of the abdominal organs HP:0002012
Genes (848)

Species:
human : 848
Page Size
Current 25
  Page 1 of 34
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanDUP17Q12100884129Chromosome 17q12 duplication syndrome
img HP RolledUp, OMIM ID: 614526
HumanSPG46100861438spastic paraplegia 46 (autosomal recessive)
img HP RolledUp, OMIM ID: 614409
HumanCCCSX100820758Cerebral-cerebellar-coloboma syndrome, X-linked
img HP RolledUp, OMIM ID: 300864
HumanDEL2Q23.1100820633
img HP RolledUp, OMIM ID: 156200
HumanMRXS17100739996Mental retardation, X-linked, syndromic 17
img HP RolledUp, OMIM ID: 300858
HumanDEL13Q14100653382Chromosome 13q14 deletion syndrome
img HP TAS, OMIM ID: 613884
HumanTRIP4Q32.1Q32.2100529228
img HP RolledUp, OMIM ID: 613603
HumanIBD11100529151Inflammatory bowel disease 11
HumanDER22T11-22100529146
img HP RolledUp, OMIM ID: 609029
HumanDEL15Q24100502567Chromosome 15q24 deletion syndrome
img HP RolledUp, OMIM ID: 613406
HumanEOE2100499167Esophagitis, eosinophilic, 2
img HP RolledUp, OMIM ID: 613412
HumanARCODS100381211Ariculocondylar syndrome
img HP RolledUp, OMIM ID: 602483
HumanPVOP1100312952Pelvic organ prolapse, susceptibility to, 1
HumanFL1100306940Follicular lymphoma, susceptibility to, 1
img HP RolledUp, OMIM ID: 613024
HumanEE100302511Esophagitis, eosinophilic
img HP RolledUp, OMIM ID: 610247
HumanCRCS10100271691Colorectal cancer, susceptibility to, 10
img HP RolledUp, OMIM ID: 612591
HumanIBD25100270799Inflammatory bowel disease-25
img HP RolledUp, OMIM ID: 612567
HumanDEL1P36100240737Chromosome 1p36 deletion syndrome
img HP RolledUp, OMIM ID: 607872
HumanDEL11P15P14100240736Chromosome 11p15-p14 deletion syndrome
img HP RolledUp, OMIM ID: 606528
HumanPLSA1100240702Primary lateral sclerosis, adult, 1
HumanIBD19100190926Inflammatory bowel disease 19
img HP RolledUp, OMIM ID: 612278
HumanDUP3Q29100188862chromosome 3q29 microduplication syndrome
img HP RolledUp, OMIM ID: 611936
HumanC22DDELS100188856Chromosome 22q11.2 deletion syndrome, distal
img HP RolledUp, OMIM ID: 611867
HumanAGSPX100188767Angio serpiginosum
img HP RolledUp, OMIM ID: 300652
HumanASDP100187749anal sphincter dysplasia
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0011024Abnormality of the gastrointestinal tract0self