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Details
Link-It Detail - Human Phenotype - Abdominal distention
Debug Stats
  • ### Total Build Time: 30 ms 27.560 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 195 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 267 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=5 ms Completed: 5 ms rowSize= 767 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 442 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 2.081 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=14 ms Completed: 14 ms rowSize= 22.688 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.015 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abdominal distention HP:0003270
Definition (1)
Abdominal distention can be a secondary feature associated with a number of conditions such as bowel obstruction.
Parents (2)
img Abnormality of the abdomen HP:0001438
img Abdominal symptom HP:0011458
Children (1)
img Protuberant abdomen HP:0001538
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 (44)

Species:
human : 44
Page Size
Current 25
  Page 1 of 2
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanBMPER168667BMP binding endothelial regulator
img HP RolledUp, OMIM ID: 608022
HumanGNPTAB79158N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits
img HP RolledUp, OMIM ID: 252500
HumanIFT12255764intraflagellar transport 122 homolog (Chlamydomonas)
img HP RolledUp, OMIM ID: 218330
HumanTRMU55687tRNA 5-methylaminomethyl-2-thiouridylate methyltransferase
img HP IEA, OMIM ID: 613070
HumanKIF1B23095kinesin family member 1B
img HP ITM, OMIM ID: 256700
HumanSEC6311231SEC63 homolog (S. cerevisiae)
img HP ITM, OMIM ID: 174050
HumanSPINT210653serine peptidase inhibitor, Kunitz type, 2
img HP IEA, OMIM ID: 270420
HumanGNE10020glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase
img HP RolledUp, OMIM ID: 269921
HumanZEB29839zinc finger E-box binding homeobox 2
img HP IEA, OMIM ID: 235730
HumanTRIP119321thyroid hormone receptor interactor 11
img HP RolledUp, OMIM ID: 200600
HumanPHOX2B8929paired-like homeobox 2b
img HP ITM, OMIM ID: 256700
img HP IEA, OMIM ID: 142623
HumanIPOX8268Intestinal pseudoobstruction, neuronal, primary idiopathic
img HP PCS, OMIM ID: 300048
HumanPAX87849paired box 8
img HP IEA, OMIM ID: 218700
HumanVDR7421vitamin D (1,25- dihydroxyvitamin D3) receptor
img HP RolledUp, OMIM ID: 277440
HumanSMPD16609sphingomyelin phosphodiesterase 1, acid lysosomal
img HP RolledUp, OMIM ID: 257200
HumanSLC2A26514solute carrier family 2 (facilitated glucose transporter), member 2
img HP IEA, OMIM ID: 227810
HumanRET5979ret proto-oncogene
img HP IEA, OMIM ID: 142623
HumanPRKCSH5589protein kinase C substrate 80K-H
img HP ITM, OMIM ID: 174050
HumanPOLG5428polymerase (DNA directed), gamma
img HP IEA, OMIM ID: 613662
HumanNRTN4902neurturin
img HP IEA, OMIM ID: 142623
HumanNPHS14868nephrosis 1, congenital, Finnish type (nephrin)
img HP IEA, OMIM ID: 256300
HumanNME14830NME/NM23 nucleoside diphosphate kinase 1
img HP ITM, OMIM ID: 256700
HumanLIPA3988lipase A, lysosomal acid, cholesterol esterase
img HP RolledUp, OMIM ID: 278000
HumanL1CAM3897L1 cell adhesion molecule
img HP IEA, OMIM ID: 142623
HumanKRT183875keratin 18
img HP IEA, OMIM ID: 215600
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0003270Abdominal distention0self