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Details
Link-It Detail - Human Phenotype - Abnormality of the esophagus
Debug Stats
  • ### Total Build Time: 46 ms 32.969 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 203 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 199 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= 800 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 5.476 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=8 ms Completed: 8 ms rowSize= 2.113 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=25 ms Completed: 25 ms rowSize= 23.039 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.022 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the esophagus HP:0002031
Definition (1)
An abnormality of the `esophagus` (FMA:7131).
Parents (2)
img Abnormality of the abdominal organs HP:0002012
img Abnormality of the gastrointestinal tract HP:0011024
Children (17)
img Esophageal atresia HP:0002032
img Tracheoesophageal fistula HP:0002575
img Esophageal diverticulum HP:0100628
img Esophageal web HP:0100594
img Barrett esophagus HP:0100580
img Esophageal duplication HP:0100681
img Esophageal stricture HP:0002043
img Dysphagia HP:0002015
img Esophageal varices HP:0002040
img Acute esophageal necrosis HP:0011128
img Esophageal neoplasm HP:0100751
img Gastroesophageal reflux HP:0002020
img Achalasia HP:0002571
img Esophageal ulceration HP:0004791
img Esophagitis HP:0100633
img Spontaneous esophageal perforation HP:0005203
img Esophageal stenosis HP:0010450
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of the abdominal organs HP:0002012
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of the gastrointestinal tract HP:0011024
Genes (261)

Species:
human : 261
Page Size
Current 25
  Page 1 of 11
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanDUP17Q12100884129Chromosome 17q12 duplication syndrome
img HP RolledUp, OMIM ID: 614526
HumanMRXS17100739996Mental retardation, X-linked, syndromic 17
img HP RolledUp, OMIM ID: 300858
HumanDER22T11-22100529146
img HP RolledUp, OMIM ID: 609029
HumanEOE2100499167Esophagitis, eosinophilic, 2
img HP RolledUp, OMIM ID: 613412
HumanARCODS100381211Ariculocondylar syndrome
img HP RolledUp, OMIM ID: 602483
HumanEE100302511Esophagitis, eosinophilic
img HP RolledUp, OMIM ID: 610247
HumanDEL1P36100240737Chromosome 1p36 deletion syndrome
img HP RolledUp, OMIM ID: 607872
HumanPLSA1100240702Primary lateral sclerosis, adult, 1
img HP RolledUp, OMIM ID: 611637
HumanAGSPX100188767Angio serpiginosum
img HP RolledUp, OMIM ID: 300652
HumanMGS100126595Mungen syndrome
img HP RolledUp, OMIM ID: 611376
HumanPTLS100038247Potocki-Lupski syndrome
img HP RolledUp, OMIM ID: 610883
HumanSCAX3727715spinocerebellar ataxia, X-linked 3
img HP RolledUp, OMIM ID: 301790
HumanATXN8724066ataxin 8
img HP RolledUp, OMIM ID: 608768
HumanPARK12677662Parkinson disease 12 (susceptibility)
img HP RolledUp, OMIM ID: 168600
HumanPSNP2619408supranuclear palsy, progressive, 2
img HP RolledUp, OMIM ID: 609454
HumanHSN1B378888Hereditary sensory neuropathy, type IB
img HP RolledUp, OMIM ID: 608088
HumanPTRF284119polymerase I and transcript release factor
img HP RolledUp, OMIM ID: 613327
HumanSYT14255928synaptotagmin XIV
img HP RolledUp, OMIM ID: 614229
HumanRFX6222546regulatory factor X, 6
img HP RolledUp, OMIM ID: 601346
HumanASXL1171023additional sex combs like 1 (Drosophila)
img HP RolledUp, OMIM ID: 605039
HumanPARK10170534Parkinson disease 10 (susceptibility)
img HP RolledUp, OMIM ID: 168600
HumanHFM170474Hemifacial microsomia
img HP RolledUp, OMIM ID: 164210
HumanARX170302aristaless related homeobox
img HP RolledUp, OMIM ID: 308350
HumanSCA19140452spinocerebellar ataxia 19
img HP RolledUp, OMIM ID: 607346
HumanAMER1139285APC membrane recruitment protein 1
img HP RolledUp, OMIM ID: 300373
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0002031Abnormality of the esophagus0self