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Details
Link-It Detail - Human Phenotype - Abdominal symptom
Debug Stats
  • ### Total Build Time: 57 ms 26.700 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 192 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=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=6 ms Completed: 6 ms rowSize= 447 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 3.221 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.162 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=45 ms Completed: 45 ms rowSize= 20.537 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.012 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abdominal symptom HP:0011458
Parents (1)
img Abnormality of the abdomen HP:0001438
Children (10)
img Nausea and vomiting HP:0002017
img Abdominal distention HP:0003270
img Malnutrition HP:0004395
img Constipation HP:0002019
img Protein avoidance HP:0002038
img Feeding difficulties HP:0011968
img Diarrhea HP:0002014
img Abdominal pain HP:0002027
img Anorexia HP:0002039
img Poor appetite HP:0004396
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001184img Abnormality of the abdomen HP:0001438
Genes (645)

Species:
human : 645
Page Size
Current 25
  Page 1 of 26
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanC16DELQ22100874527Chromosome 16q22 deletion syndrome
HumanDEL2Q23.1100820633
img HP RolledUp, OMIM ID: 156200
HumanDEL3PTERP251006533853p- syndrome
img HP RolledUp, OMIM ID: 613792
HumanDEL17P13.1100653374
img HP RolledUp, OMIM ID: 613776
HumanTRIP4Q32.1Q32.2100529228
img HP RolledUp, OMIM ID: 613603
HumanIBD11100529151Inflammatory bowel disease 11
img HP RolledUp, OMIM ID: 191390
HumanDER22T11-22100529146
img HP RolledUp, OMIM ID: 609029
HumanDEL16P12.1P11.2100526742
img HP RolledUp, OMIM ID: 613604
HumanDEL15Q24100502567Chromosome 15q24 deletion syndrome
img HP RolledUp, OMIM ID: 613406
HumanEOE2100499167Esophagitis, eosinophilic, 2
HumanDEL2P21100415942Hypotonia-cystinuria syndrome
img HP RolledUp, OMIM ID: 606407
HumanDEL19Q13.11100306978
img HP RolledUp, OMIM ID: 613026
HumanEE100302511Esophagitis, eosinophilic
HumanPRBNS100301572Pierre Robin syndrome
img HP RolledUp, OMIM ID: 261800
HumanDEL2P16.1-P15100240740
img HP RolledUp, OMIM ID: 612513
HumanDEL1P36100240737Chromosome 1p36 deletion syndrome
img HP RolledUp, OMIM ID: 607872
HumanDEL11P15P14100240736Chromosome 11p15-p14 deletion syndrome
img HP RolledUp, OMIM ID: 606528
HumanRSTSS100188814Chromosome 16p13.3 deletion syndrome
img HP RolledUp, OMIM ID: 610543
HumanCFTDX100188765Myopathy, congenital, with fiber-type disproportion, X-linked
HumanASDP100187749anal sphincter dysplasia
img HP RolledUp, OMIM ID: 105563
HumanPTLS100038247Potocki-Lupski syndrome
img HP RolledUp, OMIM ID: 610883
HumanSNORD116-1100033413
HumanPWRN1791114Prader-Willi region non-protein coding RNA 1
HumanDEL17Q21.31791085
img HP RolledUp, OMIM ID: 610443
HumanEA3780905Episodic ataxia, type 3
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0011458Abdominal symptom0self