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PedAM

Pediatric Disease Annotations & Medicines



   intussusception
  

Disease ID 1013
Disease intussusception
Definition
A form of intestinal obstruction caused by the PROLAPSE of a part of the intestine into the adjoining intestinal lumen. There are four types: colic, involving segments of the LARGE INTESTINE; enteric, involving only the SMALL INTESTINE; ileocecal, in which the ILEOCECAL VALVE prolapses into the CECUM, drawing the ILEUM along with it; and ileocolic, in which the ileum prolapses through the ileocecal valve into the COLON.
Synonym
bowel intussusception
intestinal intussusception
intestinal invagination
intestinal invaginations
intestines--intussusception
introsusception
intussuception
intussusception (disorder)
intussusception (morphologic abnormality)
intussusception [disease/finding]
intussusception nos
intussusception nos (disorder)
intussusception of intestine
intussusception of intestine (disorder)
intussusception of the intestine
intussusceptions
intususception
intususceptions
invagination of intestine
invagination of intestine or colon
invagination, intestinal
invaginations, intestinal
isn - intussusception
OMIM
DOID
ICD10
UMLS
C0021933
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:71)
C0021843  |  intestinal obstruction  |  20
C0021843  |  bowel obstruction  |  17
C0025037  |  meckel's diverticulum  |  12
C0023798  |  lipoma  |  10
C0031269  |  peutz-jeghers syndrome  |  6
C0024299  |  lymphoma  |  5
C0034888  |  rectal prolapse  |  5
C0023798  |  lipomas  |  4
C0034150  |  purpura  |  4
C0001430  |  adenoma  |  4
C0042769  |  virus infection  |  4
C0014175  |  endometriosis  |  3
C0007102  |  colon cancer  |  3
C0034152  |  henoch-schonlein purpura  |  3
C0009319  |  colitis  |  2
C0042961  |  volvulus  |  2
C0030305  |  pancreatitis  |  2
C0085693  |  acute appendicitis  |  2
C0003615  |  appendicitis  |  2
C0001418  |  adenocarcinoma  |  2
C0019829  |  hodgkin lymphoma  |  2
C0021843  |  intestinal occlusion  |  2
C0021831  |  intestinal disease  |  2
C0010346  |  crohn's disease  |  2
C0085411  |  angiodysplasia  |  2
C1258215  |  ileus  |  2
C0751498  |  sigmoid colon cancer  |  2
C0001339  |  acute pancreatitis  |  2
C0040053  |  thrombosis  |  1
C0003857  |  arteriovenous malformation  |  1
C0026691  |  kawasaki disease  |  1
C0037293  |  fibroepithelial polyp  |  1
C0206622  |  adenomyoma  |  1
C0025202  |  melanoma  |  1
C0242497  |  intestinal schistosomiasis  |  1
C0020456  |  hyperglycemia  |  1
C0001175  |  acquired immune deficiency  |  1
C0034152  |  henoch purpura  |  1
C0007113  |  rectal cancer  |  1
C0338106  |  colonic adenocarcinoma  |  1
C0021831  |  intestinal diseases  |  1
C0021400  |  influenza  |  1
C0036323  |  schistosomiasis  |  1
C0520459  |  necrotizing enterocolitis  |  1
C0282207  |  cronkhite-canada syndrome  |  1
C0278883  |  metastatic melanoma  |  1
C0009806  |  constipation  |  1
C0023267  |  fibroid  |  1
C0009324  |  ulcerative colitis  |  1
C0010674  |  cystic fibrosis  |  1
C0001175  |  acquired immune deficiency syndrome  |  1
C0031154  |  peritonitis  |  1
C0024305  |  non-hodgkin lymphoma  |  1
C0149925  |  small cell carcinoma  |  1
C0009402  |  colorectal cancer  |  1
C0020540  |  malignant hypertension  |  1
C0025037  |  meckel diverticulum  |  1
C0205697  |  sarcomatoid carcinoma  |  1
C0006413  |  burkitt lymphoma  |  1
C0008049  |  varicella  |  1
C0027726  |  nephrotic syndrome  |  1
C0016045  |  fibroma  |  1
C0026764  |  multiple myeloma  |  1
C0206632  |  angiolipoma  |  1
C0020538  |  hypertension  |  1
C0018552  |  hamartomatous  |  1
C0031269  |  peutz-jegher syndrome  |  1
C0017178  |  gastrointestinal diseases  |  1
C0017178  |  gastrointestinal disease  |  1
C0026764  |  myeloma  |  1
C0162529  |  ischemic colitis  |  1
Curated Gene(Waiting for update.)
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:100)
1080  |  CFTR  |  DISEASES
26517  |  TIMM13  |  DISEASES
57167  |  SALL4  |  DISEASES
10857  |  PGRMC1  |  DISEASES
51285  |  RASL12  |  DISEASES
3191  |  HNRNPL  |  DISEASES
973  |  CD79A  |  DISEASES
1749  |  DLX5  |  DISEASES
657  |  BMPR1A  |  DISEASES
2735  |  GLI1  |  DISEASES
3273  |  HRG  |  DISEASES
604  |  BCL6  |  DISEASES
1948  |  EFNB2  |  DISEASES
6237  |  RRAS  |  DISEASES
5880  |  RAC2  |  DISEASES
1401  |  CRP  |  DISEASES
5156  |  PDGFRA  |  DISEASES
2799  |  GNS  |  DISEASES
5159  |  PDGFRB  |  DISEASES
27130  |  INVS  |  DISEASES
22985  |  ACIN1  |  DISEASES
1  |  A1BG  |  DISEASES
57669  |  EPB41L5  |  DISEASES
3791  |  KDR  |  DISEASES
3938  |  LCT  |  DISEASES
2247  |  FGF2  |  DISEASES
6595  |  SMARCA2  |  DISEASES
2041  |  EPHA1  |  DISEASES
4851  |  NOTCH1  |  DISEASES
710  |  SERPING1  |  DISEASES
2321  |  FLT1  |  DISEASES
2911  |  GRM1  |  DISEASES
4838  |  NODAL  |  DISEASES
3815  |  KIT  |  DISEASES
50848  |  F11R  |  DISEASES
2019  |  EN1  |  DISEASES
213  |  ALB  |  DISEASES
8436  |  SDPR  |  DISEASES
2147  |  F2  |  DISEASES
947  |  CD34  |  DISEASES
7423  |  VEGFB  |  DISEASES
6794  |  STK11  |  DISEASES
400668  |  PRSS57  |  DISEASES
716  |  C1S  |  DISEASES
22906  |  TRAK1  |  DISEASES
3855  |  KRT7  |  DISEASES
6906  |  SERPINA7  |  DISEASES
2520  |  GAST  |  DISEASES
27445  |  PCLO  |  DISEASES
2246  |  FGF1  |  DISEASES
23583  |  SMUG1  |  DISEASES
1758  |  DMP1  |  DISEASES
57556  |  SEMA6A  |  DISEASES
1811  |  SLC26A3  |  DISEASES
6189  |  RPS3A  |  DISEASES
6050  |  RNH1  |  DISEASES
23481  |  PES1  |  DISEASES
55107  |  ANO1  |  DISEASES
8794  |  TNFRSF10C  |  DISEASES
50485  |  SMARCAL1  |  DISEASES
2050  |  EPHB4  |  DISEASES
404552  |  SCGB1D4  |  DISEASES
4311  |  MME  |  DISEASES
9374  |  PPT2  |  DISEASES
7058  |  THBS2  |  DISEASES
4720  |  NDUFS2  |  DISEASES
7170  |  TPM3  |  DISEASES
4288  |  MKI67  |  DISEASES
51175  |  TUBE1  |  DISEASES
5236  |  PGM1  |  DISEASES
7422  |  VEGFA  |  DISEASES
6406  |  SEMG1  |  DISEASES
2022  |  ENG  |  DISEASES
5303  |  PIN4  |  DISEASES
4146  |  MATN1  |  DISEASES
11240  |  PADI2  |  DISEASES
3376  |  IARS  |  DISEASES
7917  |  BAG6  |  DISEASES
199  |  AIF1  |  DISEASES
5293  |  PIK3CD  |  DISEASES
3980  |  LIG3  |  DISEASES
7010  |  TEK  |  DISEASES
51109  |  RDH11  |  DISEASES
388698  |  FLG2  |  DISEASES
238  |  ALK  |  DISEASES
5799  |  PTPRN2  |  DISEASES
11009  |  IL24  |  DISEASES
7122  |  CLDN5  |  DISEASES
7852  |  CXCR4  |  DISEASES
2641  |  GCG  |  DISEASES
3594  |  IL12RB1  |  DISEASES
9278  |  ZBTB22  |  DISEASES
54900  |  LAX1  |  DISEASES
56034  |  PDGFC  |  DISEASES
7033  |  TFF3  |  DISEASES
820  |  CAMP  |  DISEASES
102723508  |  KANTR  |  DISEASES
677768  |  SCARNA13  |  DISEASES
26796  |  SNORD53  |  DISEASES
100128252  |  ZNF667-AS1  |  DISEASES
Locus(Waiting for update.)
Disease ID 1013
Disease intussusception
Integrated Phenotype
HPO | Name(Total Integrated Phenotypes:1)
HP:0002576  |  Intussusception
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:53)
HP:0005214  |  Bowel obstruction  |  36
HP:0002027  |  Abdominal pain  |  13
HP:0012531  |  Pain  |  11
HP:0012032  |  Lipoma  |  10
HP:0002035  |  Rectal prolapse  |  5
HP:0002664  |  Neoplasia  |  5
HP:0002665  |  Lymphoma  |  5
HP:0000979  |  Purpura  |  3
HP:0030127  |  Endometriosis  |  3
HP:0003003  |  Colon cancer  |  3
HP:0002018  |  Nausea  |  2
HP:0002239  |  Gastrointestinal hemorrhage  |  2
HP:0100570  |  Carcinoid tumor  |  2
HP:0100723  |  Gastrointestinal stroma tumor  |  2
HP:0100822  |  Rectocele  |  2
HP:0001733  |  Pancreatic inflammation  |  2
HP:0100280  |  Morbus Crohn  |  2
HP:0012189  |  Hodgkin disease  |  2
HP:0002595  |  Gastrointestinal atony  |  2
HP:0002583  |  Colitis  |  2
HP:0002580  |  Volvulus  |  2
HP:0002584  |  Intestinal hemorrhage  |  2
HP:0001735  |  Acute pancreatitis  |  2
HP:0002013  |  Emesis  |  1
HP:0010614  |  Fibroma  |  1
HP:0002647  |  Aortic dissection  |  1
HP:0100273  |  Colon tumor  |  1
HP:0003074  |  High blood glucose  |  1
HP:0002861  |  Melanoma  |  1
HP:0100279  |  Ulcerative colitis  |  1
HP:0012721  |  Venous malformations  |  1
HP:0000822  |  Hypertension  |  1
HP:0002586  |  Peritonitis  |  1
HP:0002019  |  Dyschezia  |  1
HP:0006775  |  Multiple myeloma  |  1
HP:0000100  |  Nephrosis  |  1
HP:0001254  |  Lethargy  |  1
HP:0002607  |  Anal incontinence  |  1
HP:0011848  |  Abdominal colic  |  1
HP:0030411  |  Jejunal adenocarcinoma  |  1
HP:0002248  |  Vomitting blood  |  1
HP:0004390  |  Hamartomatous polyps  |  1
HP:0002721  |  Immunodeficiency  |  1
HP:0012539  |  Non-Hodgkin lymphoma  |  1
HP:0011458  |  Abdominal symptom  |  1
HP:0100026  |  Arteriovenous malformation  |  1
HP:0100022  |  Movement disorder  |  1
HP:0001945  |  Fever  |  1
HP:0100806  |  Sepsis  |  1
HP:0004796  |  Gastrointestinal obstruction  |  1
HP:0030080  |  Burkitt lymphoma  |  1
HP:0001696  |  Situs inversus totalis  |  1
HP:0002245  |  Meckel diverticulum  |  1
Disease ID 1013
Disease intussusception
Manually Symptom(Waiting for update.)
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:10)
C0021843  |  intestinal obstruction  |  20
C0000737  |  abdominal pain  |  13
C0235329  |  small bowel obstruction  |  12
C0034888  |  rectal prolapse  |  5
C0001486  |  adenovirus infection  |  4
C0235329  |  small intestinal obstruction  |  3
C1258215  |  ileus  |  2
C0740577  |  acute abdominal pain  |  2
C0581359  |  acute intestinal obstruction  |  1
C2004435  |  bowel ischemia  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:0)
(Waiting for update.)
GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)
GWASdb Snp Trait(Total Genotypes:0)
(Waiting for update.)
Mapped by lexical matching(Total Items:0)
(Waiting for update.)
Mapped by homologous gene(Total Items:0)
(Waiting for update.)
Chemical(Total Drugs:0)
(Waiting for update.)
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)