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Details
Link-It Detail - Human Phenotype - Abnormality of pancreas morphology
Debug Stats
  • ### Total Build Time: 49 ms 29.166 KB
  • CONCEPT_NAME gt=12 ms Completed: 12 ms rowSize= 209 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
  • 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=5 ms Completed: 5 ms rowSize= 448 bytes
  • CONCEPT_CHILDREN gt=6 ms Completed: 6 ms rowSize= 3.604 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=9 ms Completed: 9 ms rowSize= 1.163 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=15 ms Completed: 15 ms rowSize= 22.585 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.028 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of pancreas morphology HP:0012090
Parents (1)
img Abnormality of the pancreas HP:0001732
Children (11)
img Pancreatic lymphangiectasis HP:0006273
img Pancreatic calcification HP:0005213
img Pancreatic cysts HP:0001737
img Pancreatic pseudocyst HP:0005206
img Annular pancreas HP:0001734
img Ectopic pancreatic tissue HP:0006278
img Pancreatic dysplasia HP:0005232
img Pancreatic fibrosis HP:0100732
img Abnormal pancreas size HP:0012094
img Hyperechogenic pancreas HP:0006276
img Pancreatic fistula HP:0100844
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of the pancreas HP:0001732
Genes (35)

Species:
human : 35
Page Size
Current 25
  Page 1 of 2
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanDEL17Q12100884130Chromosome 17q12 deletion syndrome
img HP RolledUp, OMIM ID: 614527
HumanDEL1P36100240737Chromosome 1p36 deletion syndrome
img HP RolledUp, OMIM ID: 607872
HumanH19283120H19, imprinted maternally expressed transcript (non-protein coding)
img HP RolledUp, OMIM ID: 130650
HumanRFX6222546regulatory factor X, 6
img HP RolledUp, OMIM ID: 601346
HumanASXL1171023additional sex combs like 1 (Drosophila)
img HP RolledUp, OMIM ID: 605039
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
HumanNPHP327031nephronophthisis 3 (adolescent)
img HP RolledUp, OMIM ID: 208540
HumanCTRC11330chymotrypsin C (caldecrin)
img HP RolledUp, OMIM ID: 167800
HumanKCNQ1OT110984KCNQ1 opposite strand/antisense transcript 1 (non-protein coding)
img HP RolledUp, OMIM ID: 130650
HumanCD9610225CD96 molecule
img HP RolledUp, OMIM ID: 605039
HumanRBM8A9939RNA binding motif protein 8A
img HP RolledUp, OMIM ID: 274000
HumanEIF2AK39451eukaryotic translation initiation factor 2-alpha kinase 3
img HP RolledUp, OMIM ID: 226980
HumanRECQL49401RecQ protein-like 4
img HP RolledUp, OMIM ID: 268400
HumanOFD18481oral-facial-digital syndrome 1
img HP RolledUp, OMIM ID: 311200
HumanVHL7428von Hippel-Lindau tumor suppressor, E3 ubiquitin protein ligase
img HP RolledUp, OMIM ID: 193300
HumanHNF1B6928HNF1 homeobox B
img HP RolledUp, OMIM ID: 137920
HumanSPINK16690serine peptidase inhibitor, Kazal type 1
img HP RolledUp, OMIM ID: 167800
img HP RolledUp, OMIM ID: 608189
HumanPRSS25645protease, serine, 2 (trypsin 2)
img HP RolledUp, OMIM ID: 167800
HumanPRSS15644protease, serine, 1 (trypsin 1)
img HP RolledUp, OMIM ID: 167800
HumanPRPS15631phosphoribosyl pyrophosphate synthetase 1
img HP RolledUp, OMIM ID: 301835
HumanPKHD15314polycystic kidney and hepatic disease 1 (autosomal recessive)
img HP RolledUp, OMIM ID: 263200
HumanMYCN4613v-myc avian myelocytomatosis viral oncogene neuroblastoma derived homolog
img HP RolledUp, OMIM ID: 164280
HumanKCNQ13784potassium voltage-gated channel, KQT-like subfamily, member 1
img HP RolledUp, OMIM ID: 130650
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0012090Abnormality of pancreas morphology0self