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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine



   eosinophilic gastroenteritis
  

Disease ID 702
Disease eosinophilic gastroenteritis
Definition
Gastroenteritis that is characterized by eosinophilic infiltration.
Synonym
eosinophilic gastroent
eosinophilic gastroenteritis (disorder)
eosinophilic gastroenteropathy
eosinophilic gastroenteropathy (disorder)
eosinophilic gastroenteropathy, nos
gastroenteritis eosinophilic
Orphanet
DOID
UMLS
C1262481
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:16)
C0002871  |  anemia  |  1
C0024623  |  gastric cancer  |  1
C0004096  |  asthma  |  1
C0015645  |  fasciitis  |  1
C0024141  |  systemic lupus erythematosus  |  1
C0019196  |  hepatitis c  |  1
C0019158  |  hepatitis  |  1
C0155877  |  allergic asthma  |  1
C0023890  |  cirrhosis  |  1
C0006277  |  bronchitis  |  1
C0206141  |  hypereosinophilic syndrome  |  1
C0409974  |  lupus erythematosus  |  1
C0008728  |  churg-strauss syndrome  |  1
C0023890  |  liver cirrhosis  |  1
C0003873  |  rheumatoid arthritis  |  1
C0013292  |  duodenal obstruction  |  1
Curated Gene(Waiting for update.)
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:11)
58  |  ACTA1  |  1.641  |  DISEASES
1232  |  CCR3  |  1.496  |  DISEASES
1103  |  CHAT  |  1.167  |  DISEASES
81608  |  FIP1L1  |  3.229  |  DISEASES
388698  |  FLG2  |  2.686  |  DISEASES
55340  |  GIMAP5  |  2.797  |  DISEASES
2875  |  GPT  |  2.359  |  DISEASES
90865  |  IL33  |  1.27  |  DISEASES
5265  |  SERPINA1  |  1.246  |  DISEASES
7052  |  TGM2  |  1.81  |  DISEASES
85480  |  TSLP  |  2.261  |  DISEASES
Locus(Waiting for update.)
Disease ID 702
Disease eosinophilic gastroenteritis
Integrated Phenotype
HPO | Name(Total Integrated Phenotypes:19)
HP:0002243  |  Protein-losing enteropathy
HP:0001974  |  Leukocytosis
HP:0003565  |  Elevated erythrocyte sedimentation rate
HP:0002570  |  Steatorrhea
HP:0002013  |  Vomiting
HP:0001047  |  Atopic dermatitis
HP:0002014  |  Diarrhea
HP:0002015  |  Dysphagia
HP:0003193  |  Allergic rhinitis
HP:0002027  |  Abdominal pain
HP:0001824  |  Weight loss
HP:0011227  |  Elevated C-reactive protein level
HP:0002573  |  Hematochezia
HP:0001541  |  Ascites
HP:0002099  |  Asthma
HP:0003073  |  Hypoalbuminemia
HP:0001903  |  Anemia
HP:0002024  |  Malabsorption
HP:0000969  |  Edema
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:14)
HP:0001541  |  Ascites  |  4
HP:0001903  |  Anemia  |  1
HP:0005240  |  Esophageal obstruction  |  1
HP:0002099  |  Asthma  |  1
HP:0002240  |  Enlarged liver  |  1
HP:0012115  |  Liver inflammation  |  1
HP:0005202  |  Helicobacter pylori infection  |  1
HP:0002725  |  Systemic lupus erythematosus  |  1
HP:0012387  |  Bronchitis  |  1
HP:0200123  |  Chronic liver inflammation  |  1
HP:0001370  |  Rheumatoid arthritis  |  1
HP:0012126  |  Gastric cancer  |  1
HP:0001394  |  Hepatic cirrhosis  |  1
HP:0100537  |  Inflammation of the fascia  |  1
Disease ID 702
Disease eosinophilic gastroenteritis
Manually Symptom
UMLS  | Name(Total Manually Symptoms:14)
C2632116  |  stenosis
C1699656  |  jejunal obstruction
C1527407  |  eosinophilic pneumonia
C1443924  |  severe diarrhea
C0744421  |  immune complex glomerulonephritis
C0742965  |  eosinophilic cystitis
C0400979  |  biliary obstruction
C0348024  |  thyroid dysfunction
C0267937  |  recurrent acute pancreatitis
C0267448  |  eosinophilic colitis
C0034194  |  pyloric stenosis
C0021845  |  intestinal perforation
C0013395  |  dyspepsia
C0000727  |  acute abdomen
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:1)
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
Text Mining Genotype(Total 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:4)
HP ID HP Name MP ID MP Name Annotation
HP:0011227Elevated C-reactive protein levelMP:0008721abnormal chemokine leveldeviation from the normal levels of any of the class of pro-inflammatory cytokines that attract and activate leukocytes
HP:0003565Elevated erythrocyte sedimentation rateMP:0008770decreased survivor ratea smaller percentage of organisms than expected survive to adulthood and have a lifespan similar to controls
HP:0001047Atopic dermatitisMP:0001194dermatitisinflammation of the skin (redness and itching) caused by an allergic reaction or contact with an irritant
HP:0001824Weight lossMP:0005114premature hair lossrelease of fur at an earlier than expected time
Mapped by homologous gene(Total Items:19)
HP ID HP Name MP ID MP Name Annotation
HP:0002099AsthmaMP:0020254decreased collagen leveldecreased level of the main structural protein of the various connective tissues in animals
HP:0003193Allergic rhinitisMP:0012080chylous ascitesthe extravasation of milky triglyceride-rich chyle into the peritoneal cavity; often a secondary symptom of neoplasms
HP:0001824Weight lossMP:0020220decreased tear productiondecreased production of the amount of fluid produced in the eye
HP:0000969EdemaMP:0020154impaired humoral immune responseimpaired response of the immune system that mediates secreted antibodies produced in B cells
HP:0002013VomitingMP:0020316decreased vascular endothelial cell proliferationdecrease in the expansion rate of any vascular endothelial cell population by cell division
HP:0002027Abdominal painMP:0020220decreased tear productiondecreased production of the amount of fluid produced in the eye
HP:0001047Atopic dermatitisMP:0020154impaired humoral immune responseimpaired response of the immune system that mediates secreted antibodies produced in B cells
HP:0001974LeukocytosisMP:0020154impaired humoral immune responseimpaired response of the immune system that mediates secreted antibodies produced in B cells
HP:0002570SteatorrheaMP:0020137decreased bone mineralizationdecrease in the rate at which minerals are deposited into bone
HP:0002015DysphagiaMP:0020329decreased capillary densityreduction in the number of capillaries in a given cross-sectional area of a tissue
HP:0003073HypoalbuminemiaMP:0020215impaired blood coagulationimpaired ability of the blood to clot
HP:0002243Protein-losing enteropathyMP:0013504increased embryonic tissue cell apoptosisincrease in the timing or the number of cells in embryonic tissue undergoing programmed cell death
HP:0002014DiarrheaMP:0020220decreased tear productiondecreased production of the amount of fluid produced in the eye
HP:0001541AscitesMP:0020137decreased bone mineralizationdecrease in the rate at which minerals are deposited into bone
HP:0002024MalabsorptionMP:0020220decreased tear productiondecreased production of the amount of fluid produced in the eye
HP:0002573HematocheziaMP:0013745abnormal eyelid margin morphologyany structural anomaly of the confluence of the mucosal surface of the conjunctiva, the edge of the orbicularis, and the cutaneous epithelium
HP:0001903AnemiaMP:0020316decreased vascular endothelial cell proliferationdecrease in the expansion rate of any vascular endothelial cell population by cell division
HP:0003565Elevated erythrocyte sedimentation rateMP:0020154impaired humoral immune responseimpaired response of the immune system that mediates secreted antibodies produced in B cells
HP:0011227Elevated C-reactive protein levelMP:0008721abnormal chemokine leveldeviation from the normal levels of any of the class of pro-inflammatory cytokines that attract and activate leukocytes
Disease ID 702
Disease eosinophilic gastroenteritis
Case(Waiting for update.)