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Details
Link-It Detail - Human Phenotype - Abnormality of the pancreas
Debug Stats
  • ### Total Build Time: 230 ms 32.760 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= 198 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= 456 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 6.193 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.171 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=220 ms Completed: 220 ms rowSize= 23.394 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 the pancreas HP:0001732
Definition (1)
An abnormality of the `pancreas` (FMA:7198).
Parents (1)
img Abnormality of the abdominal organs HP:0002012
Children (19)
img Pancreatic lymphangiectasis HP:0006273
img Pancreatic insufficiency HP:0002581
img Pancreatic calcification HP:0005213
img Aplasia/Hypoplasia of the pancreas HP:0100800
img Pancreatic cysts HP:0001737
img Pancreatic pseudocyst HP:0005206
img Pancreatitis HP:0001733
img Annular pancreas HP:0001734
img Abnormality of the pancreatic islet cells HP:0006476
img Ectopic pancreatic tissue HP:0006278
img Pancreatic hypoplasia HP:0002594
img Pancreatic dysplasia HP:0005232
img Neoplasm of the pancreas HP:0002894
img Pancreatic hyperplasia HP:0006277
img Abnormality of pancreas morphology HP:0012090
img Pancreatic fibrosis HP:0100732
img Hyperechogenic pancreas HP:0006276
img Abnormality of pancreas physiology HP:0012091
img Pancreatic fistula HP:0100844
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of the abdominal organs HP:0002012
Genes (127)

Species:
human : 127
Page Size
Current 25
  Page 1 of 6
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanDEL17Q12100884130Chromosome 17q12 deletion syndrome
img HP RolledUp, OMIM ID: 614527
HumanDEL1P36100240737Chromosome 1p36 deletion syndrome
img HP RolledUp, OMIM ID: 607872
HumanWG474168Wegener granulomatosis
img HP RolledUp, OMIM ID: 608710
HumanH19283120H19, imprinted maternally expressed transcript (non-protein coding)
img HP RolledUp, OMIM ID: 130650
HumanITS282551Insulinoma tumor suppressor gene locus
img HP RolledUp, OMIM ID: 606960
HumanPTF1A256297pancreas specific transcription factor, 1a
img HP TAS, OMIM ID: 609069
HumanRFX6222546regulatory factor X, 6
img HP RolledUp, OMIM ID: 601346
HumanUBR1197131ubiquitin protein ligase E3 component n-recognin 1
img HP RolledUp, OMIM ID: 243800
HumanASXL1171023additional sex combs like 1 (Drosophila)
img HP TAS, OMIM ID: 605039
HumanARX170302aristaless related homeobox
img HP RolledUp, OMIM ID: 300215
HumanDIS3L2129563DIS3 mitotic control homolog (S. cerevisiae)-like 2
img HP TAS, OMIM ID: 267000
HumanCDC7379577cell division cycle 73
img HP IEA, OMIM ID: 145001
HumanNSD164324nuclear receptor binding SET domain protein 1
img HP RolledUp, OMIM ID: 130650
HumanSTRA664220stimulated by retinoic acid 6
img HP RolledUp, OMIM ID: 601186
HumanXPNPEP363929X-prolyl aminopeptidase (aminopeptidase P) 3, putative
img HP RolledUp, OMIM ID: 613159
HumanSBDS51119Shwachman-Bodian-Diamond syndrome
img HP RolledUp, OMIM ID: 260400
HumanNPHP327031nephronophthisis 3 (adolescent)
img HP RolledUp, OMIM ID: 208540
img HP TAS, OMIM ID: 267010
HumanBSCL226580Berardinelli-Seip congenital lipodystrophy 2 (seipin)
img HP RolledUp, OMIM ID: 269700
HumanPALLD23022palladin, cytoskeletal associated protein
img HP RolledUp, OMIM ID: 260350
HumanCTRC11330chymotrypsin C (caldecrin)
img HP RolledUp, OMIM ID: 167800
HumanSEC6311231SEC63 homolog (S. cerevisiae)
img HP TAS, OMIM ID: 174050
HumanKCNQ1OT110984KCNQ1 opposite strand/antisense transcript 1 (non-protein coding)
img HP RolledUp, OMIM ID: 130650
HumanAGPAT2105551-acylglycerol-3-phosphate O-acyltransferase 2
img HP RolledUp, OMIM ID: 608594
HumanCD9610225CD96 molecule
img HP TAS, OMIM ID: 605039
HumanSLC25A1310165solute carrier family 25 (aspartate/glutamate carrier), member 13
img HP RolledUp, OMIM ID: 603471
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0001732Abnormality of the pancreas0self