ONTOLOGY REPORT - ANNOTATIONS


Term:ileus
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Accession:DOID:8440 term browser browse the term
Definition:A condition caused by the lack of intestinal PERISTALSIS or INTESTINAL MOTILITY without any mechanical obstruction. This interference of the flow of INTESTINAL CONTENTS often leads to INTESTINAL OBSTRUCTION. Ileus may be classified into postoperative, inflammatory, metabolic, neurogenic, and drug-induced.
Synonyms:exact_synonym: Ileus of intestine
 primary_id: MESH:D045823;   RDO:0005902
For additional species annotation, visit the Alliance of Genome Resources.


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ileus term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Hmox1 heme oxygenase 1 JBrowse link 19 14,508,634 14,515,455 RGD:10755726
G Mmp9 matrix metallopeptidase 9 JBrowse link 3 161,413,410 161,421,473 RGD:8547906
chronic atrial and intestinal dysrhythmia term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Sgo1 shugoshin 1 JBrowse link 9 4,420,158 4,435,939 RGD:8554872
RGD:7240710
Congenital Idiopathic Intestinal Pseudoobstruction term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Flna filamin A JBrowse link X 156,460,785 156,487,245 RGD:7240710
RGD:8554872
Familial Visceral Myopathy term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Actg2 actin gamma 2, smooth muscle JBrowse link 4 115,215,160 115,239,746 RGD:11554173
Familial Visceral Neuropathy, Autosomal Dominant term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Actg2 actin gamma 2, smooth muscle JBrowse link 4 115,215,160 115,239,746 RGD:8554872
intestinal pseudo-obstruction term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Actg2 actin gamma 2, smooth muscle JBrowse link 4 115,215,160 115,239,746 RGD:8554872
G Clmp CXADR-like membrane protein JBrowse link 8 44,846,685 44,975,460 RGD:8554872
RGD:7240710
G Flna filamin A JBrowse link X 156,460,785 156,487,245 RGD:8554872
G Lmod1 leiomodin 1 JBrowse link 13 52,147,099 52,189,835 RGD:8554872
G Myh11 myosin heavy chain 11 JBrowse link 10 764,421 859,184 RGD:8554872
G Myl9 myosin light chain 9 JBrowse link 3 152,857,573 152,863,961 RGD:8554872
G Mylk myosin light chain kinase JBrowse link 11 69,013,060 69,260,039 RGD:8554872
G Nup35 nucleoporin 35 JBrowse link 3 67,866,784 67,896,828 RGD:13592920
G Pten phosphatase and tensin homolog JBrowse link 1 251,421,814 251,487,634 RGD:13592920
G Rb1 RB transcriptional corepressor 1 JBrowse link 15 55,081,582 55,209,060 RGD:8547979
Meconium Ileus term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Gucy2c guanylate cyclase 2C JBrowse link 4 170,659,993 170,740,274 RGD:7240710
RGD:8554872
G LOC500354 similar to C030030A07Rik protein JBrowse link 4 170,807,633 170,822,514 RGD:8554872
megacystis-microcolon-intestinal hypoperistalsis syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Actg2 actin gamma 2, smooth muscle JBrowse link 4 115,215,160 115,239,746 RGD:8554872
RGD:7240710
RGD:11554173
G Chrm3 cholinergic receptor, muscarinic 3 JBrowse link 17 63,990,599 64,463,222 RGD:13592920
G Lmod1 leiomodin 1 JBrowse link 13 52,147,099 52,189,835 RGD:7240710
mitochondrial DNA depletion syndrome 8A term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Ncaph2 non-SMC condensin II complex, subunit H2 JBrowse link 7 130,326,597 130,343,655 RGD:8554872
G Polg DNA polymerase gamma, catalytic subunit JBrowse link 1 141,172,117 141,188,893 RGD:8554872
G Rrm2b ribonucleotide reductase regulatory TP53 inducible subunit M2B JBrowse link 7 76,750,045 76,780,817 RGD:8554872
RGD:7240710
G Tymp thymidine phosphorylase JBrowse link 7 130,342,481 130,347,845 RGD:8554872
Mungan Syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Rad21 RAD21 cohesin complex component JBrowse link 7 91,511,755 91,538,673 RGD:7240710
RGD:8554872
X-Linked Hydrocephalus, with Congenital Idiopathic Intestinal Pseudoobstruction term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G L1cam L1 cell adhesion molecule JBrowse link X 156,901,244 156,928,064 RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14919
    disease of anatomical entity 14083
      gastrointestinal system disease 4264
        intestinal disease 1311
          intestinal obstruction 31
            ileus 22
              Meconium Ileus 2
              intestinal pseudo-obstruction + 18
              paralytic ileus 0
Path 2
Term Annotations click to browse term
  disease 14919
    disease of anatomical entity 14083
      gastrointestinal system disease 4264
        Gastrointestinal Diseases 2359
          intestinal disease 1311
            intestinal obstruction 31
              ileus 22
                Meconium Ileus 2
                intestinal pseudo-obstruction + 18
                paralytic ileus 0
paths to the root

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.