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Pediatric Disease Annotations & Medicines



   giardiasis
  

Disease ID 1279
Disease giardiasis
Definition
An infection of the SMALL INTESTINE caused by the flagellated protozoan GIARDIA LAMBLIA. It is spread via contaminated food and water and by direct person-to-person contact.
Synonym
colitis - giardial
giardial colitis
giardial enteritis
giardiases
giardiasis (& [colitis])
giardiasis (& [colitis]) (disorder)
giardiasis (disorder)
giardiasis - lambliasis
giardiasis [ambiguous]
giardiasis [disease/finding]
giardiasis intestinal
giardiasis: [lambliasis] or [colitis]
giardiasis: [lambliasis] or [colitis] (disorder)
giardiosis
infection by giardia lamblia
infection by giardia lamblia (disorder)
infection caused by giardia lamblia
infection caused by giardia lamblia (disorder)
intestinal giardiasis
lambliases
lambliasis
DOID
UMLS
C0017536
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:21)
C0011991  |  diarrhea  |  8
C0024523  |  malabsorption  |  4
C0011849  |  diabetes mellitus  |  1
C0008728  |  churg-strauss syndrome  |  1
C0010418  |  cryptosporidiosis  |  1
C0003950  |  ascariasis  |  1
C0021831  |  enteropathy  |  1
C0162316  |  iron deficiency anemia  |  1
C0005684  |  bladder cancer  |  1
C0747256  |  parasitic infection  |  1
C0033680  |  protein-losing enteropathy  |  1
C0038463  |  strongyloidiasis  |  1
C0017178  |  gastrointestinal disorder  |  1
C0020413  |  hymenolepiasis  |  1
C0013395  |  dyspepsia  |  1
C0016412  |  folate deficiency  |  1
C0017178  |  gastrointestinal disorders  |  1
C0022951  |  lactose intolerance  |  1
C0153452  |  gallbladder cancer  |  1
C0011847  |  diabetes  |  1
C0153452  |  gallbladder ca  |  1
Curated Gene(Waiting for update.)
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:1)
7040  |  TGFB1  |  infer
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:80)
479  |  ATP12A  |  DISEASES
54623  |  PAF1  |  DISEASES
1158  |  CKM  |  DISEASES
973  |  CD79A  |  DISEASES
6528  |  SLC5A5  |  DISEASES
230  |  ALDOC  |  DISEASES
7167  |  TPI1  |  DISEASES
3565  |  IL4  |  DISEASES
2023  |  ENO1  |  DISEASES
8317  |  CDC7  |  DISEASES
7166  |  TPH1  |  DISEASES
10955  |  SERINC3  |  DISEASES
3569  |  IL6  |  DISEASES
10241  |  CALCOCO2  |  DISEASES
495  |  ATP4A  |  DISEASES
3938  |  LCT  |  DISEASES
80725  |  SRCIN1  |  DISEASES
23395  |  LARS2  |  DISEASES
10926  |  DBF4  |  DISEASES
6523  |  SLC5A1  |  DISEASES
4123  |  MAN2C1  |  DISEASES
150094  |  SIK1  |  DISEASES
963  |  CD53  |  DISEASES
7082  |  TJP1  |  DISEASES
115584  |  SLC5A11  |  DISEASES
3099  |  HK2  |  DISEASES
3101  |  HK3  |  DISEASES
1990  |  CELA1  |  DISEASES
6006  |  RHCE  |  DISEASES
886  |  CCKAR  |  DISEASES
213  |  ALB  |  DISEASES
3251  |  HPRT1  |  DISEASES
3906  |  LALBA  |  DISEASES
3308  |  HSPA4  |  DISEASES
56246  |  MRAP  |  DISEASES
836  |  CASP3  |  DISEASES
92745  |  SLC38A5  |  DISEASES
2193  |  FARSA  |  DISEASES
1670  |  DEFA5  |  DISEASES
6007  |  RHD  |  DISEASES
3320  |  HSP90AA1  |  DISEASES
887  |  CCKBR  |  DISEASES
226  |  ALDOA  |  DISEASES
23436  |  CELA3B  |  DISEASES
11188  |  NISCH  |  DISEASES
126364  |  LRRC25  |  DISEASES
25870  |  SUMF2  |  DISEASES
1364  |  CLDN4  |  DISEASES
347  |  APOD  |  DISEASES
1861  |  TOR1A  |  DISEASES
100506658  |  OCLN  |  DISEASES
5284  |  PIGR  |  DISEASES
2224  |  FDPS  |  DISEASES
51592  |  TRIM33  |  DISEASES
5893  |  RAD52  |  DISEASES
5116  |  PCNT  |  DISEASES
4638  |  MYLK  |  DISEASES
7096  |  TLR1  |  DISEASES
5406  |  PNLIP  |  DISEASES
959  |  CD40LG  |  DISEASES
1056  |  CEL  |  DISEASES
93643  |  TJAP1  |  DISEASES
229  |  ALDOB  |  DISEASES
11240  |  PADI2  |  DISEASES
6518  |  SLC2A5  |  DISEASES
10333  |  TLR6  |  DISEASES
7932  |  OR2H2  |  DISEASES
51343  |  FZR1  |  DISEASES
3098  |  HK1  |  DISEASES
2935  |  GSPT1  |  DISEASES
7124  |  TNF  |  DISEASES
1018  |  CDK3  |  DISEASES
2821  |  GPI  |  DISEASES
3586  |  IL10  |  DISEASES
51071  |  DERA  |  DISEASES
4700  |  NDUFA6  |  DISEASES
246744  |  STH  |  DISEASES
54937  |  SOHLH2  |  DISEASES
246734  |  NPCDR1  |  DISEASES
100302740  |  FAS-AS1  |  DISEASES
Locus(Waiting for update.)
Disease ID 1279
Disease giardiasis
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:17)
HP:0002014  |  Diarrhea  |  8
HP:0002024  |  Intestinal malabsorption  |  4
HP:0002028  |  Chronic diarrhea  |  2
HP:0001548  |  Overgrowth  |  1
HP:0002202  |  Pleural effusion  |  1
HP:0002243  |  Protein-losing enteropathy  |  1
HP:0001891  |  Iron-deficiency anemia  |  1
HP:0100507  |  Folate deficiency  |  1
HP:0009725  |  Bladder neoplasm  |  1
HP:0002242  |  Enteropathy  |  1
HP:0004789  |  Lactose intolerance  |  1
HP:0001880  |  Eosinophilia  |  1
HP:0000819  |  Diabetes mellitus  |  1
HP:0001824  |  Weight loss  |  1
HP:0000787  |  Renal calculi  |  1
HP:0002027  |  Abdominal pain  |  1
HP:0012531  |  Pain  |  1
Disease ID 1279
Disease giardiasis
Manually Symptom(Waiting for update.)
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:6)
C0011991  |  diarrhea  |  8
C0024523  |  malabsorption  |  4
C0016412  |  folate deficiency  |  1
C0009450  |  infection  |  1
C0426576  |  gastrointestinal symptoms  |  1
C0033680  |  protein-losing enteropathy  |  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:2)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0017536albendazoleD01576654965-21-8giardiasisMESH:D005873therapeutic17333792
C0017536furazolidoneD00566467-45-8giardiasisMESH:D005873therapeutic9564507
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)