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PedAM

Pediatric Disease Annotations & Medicines



   intestinal pseudo-obstruction
  

Disease ID 851
Disease intestinal pseudo-obstruction
Definition
A type of ILEUS, a functional not mechanical obstruction of the INTESTINES. This syndrome is caused by a large number of disorders involving the smooth muscles (MUSCLE, SMOOTH) or the NERVOUS SYSTEM.
Synonym
chronic idiopathic intestinal pseudo-obstruction
congenital short bowel syndrome
congenital short bowel syndrome (disorder)
csbs
enteric neuropathy
idiopathic intestinal pseudo-obstruction
idiopathic intestinal pseudo-obstructions
intestinal pseudo obstruction
intestinal pseudo obstruction, idiopathic
intestinal pseudo-obstruction [disease/finding]
intestinal pseudo-obstruction, idiopathic
intestinal pseudo-obstructions
intestinal pseudo-obstructions, idiopathic
intestinal pseudoobstruction
intestinal pseudoobstructions
intestine pseudoobstruction
intestine, pseudoobstruction
pseudo intestinal obstruction
pseudo obstruction intestinal
pseudo obstruction, intestinal
pseudo-obstruction of intestine
pseudo-obstruction of intestine (disorder)
pseudo-obstruction, idiopathic intestinal
pseudo-obstruction, intestinal
pseudo-obstructions, idiopathic intestinal
pseudo-obstructions, intestinal
pseudointestinal obstruction syndrome
pseudoobstruction, intestinal
pseudoobstructions, intestinal
pseudoobstructive syndrome
Orphanet
OMIM
DOID
UMLS
C0021847
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:13)
C0409974  |  lupus erythematosus  |  3
C0024141  |  systemic lupus erythematosus  |  3
C0042961  |  volvulus  |  2
C0014848  |  achalasia  |  2
C0751651  |  mitochondrial disease  |  1
C0025160  |  megacolon  |  1
C0013473  |  eating disorder  |  1
C0152020  |  gastroparesis  |  1
C0751651  |  mitochondrial diseases  |  1
C0036421  |  systemic sclerosis  |  1
C0442874  |  neuropathy  |  1
C0031511  |  phaeochromocytoma  |  1
C0026691  |  kawasaki disease  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:2)
FLNA  |  2316  |  ORPHANET;GHR
CLMP  |  79827  |  CLINVAR;ORPHANET;UNIPROT
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:83)
2767  |  GNA11  |  DISEASES
28954  |  REM1  |  DISEASES
49  |  ACR  |  DISEASES
2862  |  MLNR  |  DISEASES
2765  |  GML  |  DISEASES
59  |  ACTA2  |  DISEASES
79176  |  FBXL15  |  DISEASES
5539  |  PPY  |  DISEASES
2798  |  GNRHR  |  DISEASES
2026  |  ENO2  |  DISEASES
55907  |  CMAS  |  DISEASES
3196  |  TLX2  |  DISEASES
2797  |  GNRH2  |  DISEASES
1890  |  TYMP  |  DISEASES
1264  |  CNN1  |  DISEASES
3110  |  MNX1  |  DISEASES
6535  |  SLC6A8  |  DISEASES
6741  |  SSB  |  DISEASES
2294  |  FOXF1  |  DISEASES
3249  |  HPN  |  DISEASES
2769  |  GNA15  |  DISEASES
6855  |  SYP  |  DISEASES
590  |  BCHE  |  DISEASES
6722  |  SRF  |  DISEASES
8829  |  NRP1  |  DISEASES
5428  |  POLG  |  DISEASES
6876  |  TAGLN  |  DISEASES
83706  |  FERMT3  |  DISEASES
7345  |  UCHL1  |  DISEASES
6750  |  SST  |  DISEASES
3815  |  KIT  |  DISEASES
56896  |  DPYSL5  |  DISEASES
3973  |  LHCGR  |  DISEASES
129401  |  NUP35  |  DISEASES
72  |  ACTG2  |  DISEASES
213  |  ALB  |  DISEASES
10653  |  SPINT2  |  DISEASES
43  |  ACHE  |  DISEASES
794  |  CALB2  |  DISEASES
5644  |  PRSS1  |  DISEASES
8557  |  TCAP  |  DISEASES
2744  |  GLS  |  DISEASES
6331  |  SCN5A  |  DISEASES
51738  |  GHRL  |  DISEASES
885  |  CCK  |  DISEASES
1908  |  EDN3  |  DISEASES
3363  |  HTR7  |  DISEASES
6609  |  SMPD1  |  DISEASES
1431  |  CS  |  DISEASES
132884  |  EVC2  |  DISEASES
1760  |  DMPK  |  DISEASES
7453  |  WARS  |  DISEASES
1785  |  DNM2  |  DISEASES
5979  |  RET  |  DISEASES
6525  |  SMTN  |  DISEASES
1995  |  ELAVL3  |  DISEASES
4638  |  MYLK  |  DISEASES
3360  |  HTR4  |  DISEASES
6663  |  SOX10  |  DISEASES
7432  |  VIP  |  DISEASES
9446  |  GSTO1  |  DISEASES
2316  |  FLNA  |  DISEASES
3897  |  L1CAM  |  DISEASES
3195  |  TLX1  |  DISEASES
959  |  CD40LG  |  DISEASES
81030  |  ZBP1  |  DISEASES
4303  |  FOXO4  |  DISEASES
229  |  ALDOB  |  DISEASES
1910  |  EDNRB  |  DISEASES
54840  |  APTX  |  DISEASES
4629  |  MYH11  |  DISEASES
6314  |  ATXN7  |  DISEASES
3778  |  KCNMA1  |  DISEASES
4295  |  MLN  |  DISEASES
93649  |  MYOCD  |  DISEASES
9278  |  ZBTB22  |  DISEASES
79827  |  CLMP  |  DISEASES
7019  |  TFAM  |  DISEASES
136541  |  PRSS58  |  DISEASES
567  |  B2M  |  DISEASES
6625  |  SNRNP70  |  DISEASES
102723508  |  KANTR  |  DISEASES
4567  |  MT-TL1  |  DISEASES
Locus(Waiting for update.)
Disease ID 851
Disease intestinal pseudo-obstruction
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:9)
HP:0002725  |  Systemic lupus erythematosus  |  3
HP:0002251  |  Hirschsprung megacolon  |  3
HP:0002571  |  Achalasia  |  2
HP:0002580  |  Volvulus  |  2
HP:0001541  |  Ascites  |  1
HP:0002015  |  Swallowing difficulty  |  1
HP:0011947  |  Respiratory infection  |  1
HP:0000155  |  Oral ulcer  |  1
HP:0002578  |  Gastroparesis  |  1
Disease ID 851
Disease intestinal pseudo-obstruction
Manually Symptom(Waiting for update.)
Text Mined Symptom(Waiting for update.)
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:4)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs587776964NA79827CLMPumls:C0021847CLINVARNA0.240542884NACLMP;LOC10192928911123084670T-
rs587776965NA79827CLMPumls:C0021847CLINVARNA0.240542884NACLMP;LOC10192928911123074702CT
rs587776966NA79827CLMPumls:C0021847CLINVARNA0.240542884NACLMP;LOC10192928911123083100GA
rs587776967NA79827CLMPumls:C0021847CLINVARNA0.240542884NACLMP;LOC10192928911123084529AT
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:3)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0021847clozapineD0030245786-21-0intestinal pseudo-obstructionMESH:D007418marker/mechanism1860384
C0021847vincristineD014750-intestinal pseudo-obstructionMESH:D007418marker/mechanism9434832
C0021847vindesineD01475153643-48-4intestinal pseudo-obstructionMESH:D007418marker/mechanism17617780
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)