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Details
Link-It Detail - Human Phenotype - Abnormality of the intestine
Debug Stats
  • ### Total Build Time: 50 ms 35.433 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 203 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 276 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
  • CONCEPT_NAMESPACE gt=NONE 1 ms Completed: 1 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 800 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 8.692 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.113 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=43 ms Completed: 43 ms rowSize= 22.211 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.022 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the intestine HP:0002242
Definition (1)
The intestine (also known as bowel) is comprised of the `small intestine` (FMA:7200) and the `large intestine` (FMA:7201).
Parents (2)
img Abnormality of the abdominal organs HP:0002012
img Abnormality of the gastrointestinal tract HP:0011024
Children (27)
img Constipation HP:0002019
img Intussusception HP:0002576
img Bowel diverticulosis HP:0005222
img Intestinal pseudo-obstruction HP:0004389
img Intestinal fistula HP:0100819
img Multiple intestinal neurofibromatosis HP:0005220
img Intestinal edema HP:0005225
img Abnormality of the large intestine HP:0002250
img Diarrhea HP:0002014
img Malabsorption HP:0002024
img Intestinal polyps HP:0005266
img Intestinal malrotation HP:0002566
img Intestinal hypoplasia HP:0005245
img Abnormality of the small intestine HP:0002244
img Volvulus HP:0002580
img Abnormality of the peritoneum HP:0002585
img Intestinal lymphangiectasia HP:0002593
img Echogenic fetal bowel HP:0010943
img Intestinal lymphoid nodular hyperplasia HP:0011956
img Intestinal lymphedema HP:0004788
img Intestinal bleeding HP:0002584
img Abnormality of the enteric ganglia HP:0004362
img Enteropathy HP:0002628
img Inflammation of the large intestine HP:0002037
img Ileus HP:0002595
img Intestinal atresia HP:0011100
img Intestinal duplication HP:0100668
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 (574)

Species:
human : 574
Page Size
Current 25
  Page 1 of 23
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanSPG46100861438spastic paraplegia 46 (autosomal recessive)
img HP RolledUp, OMIM ID: 614409
HumanCCCSX100820758Cerebral-cerebellar-coloboma syndrome, X-linked
img HP RolledUp, OMIM ID: 300864
HumanDEL2Q23.1100820633
img HP RolledUp, OMIM ID: 156200
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
HumanPVOP1100312952Pelvic organ prolapse, susceptibility to, 1
img HP RolledUp, OMIM ID: 176780
HumanFL1100306940Follicular lymphoma, susceptibility to, 1
img HP RolledUp, OMIM ID: 613024
HumanCRCS10100271691Colorectal cancer, susceptibility to, 10
img HP RolledUp, OMIM ID: 612591
HumanIBD25100270799Inflammatory bowel disease-25
img HP RolledUp, OMIM ID: 612567
HumanDEL1P36100240737Chromosome 1p36 deletion syndrome
img HP TAS, OMIM ID: 607872
HumanDEL11P15P14100240736Chromosome 11p15-p14 deletion syndrome
img HP IEA, OMIM ID: 606528
HumanIBD19100190926Inflammatory bowel disease 19
img HP RolledUp, OMIM ID: 612278
HumanC22DDELS100188856Chromosome 22q11.2 deletion syndrome, distal
img HP RolledUp, OMIM ID: 611867
HumanASDP100187749anal sphincter dysplasia
img HP RolledUp, OMIM ID: 105563
HumanCD24100133941CD24 molecule
HumanMGS100126595Mungen syndrome
img HP RolledUp, OMIM ID: 611376
HumanSPG37100049159spastic paraplegia 37 (autosomal dominant)
HumanSPG36791228spastic paraplegia 36 (autosomal dominant)
img HP RolledUp, OMIM ID: 613096
HumanHHT4791087Telangiectasia, hereditary hemorrhagic, type 4
img HP RolledUp, OMIM ID: 610655
HumanPARK12677662Parkinson disease 12 (susceptibility)
img HP RolledUp, OMIM ID: 168600
HumanNCF1653361neutrophil cytosolic factor 1
img HP RolledUp, OMIM ID: 233700
HumanWTRS619509Wittwer syndrome
img HP RolledUp, OMIM ID: 300421
HumanSPG29619379spastic paraplegia 29 (autosomal dominant)
HumanCDAGS574043Craniosynostosis, anal anomalies, and porokeratosis syndrome
img HP RolledUp, OMIM ID: 603116
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0002242Abnormality of the intestine0self