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Pediatric Disease Annotations & Medicines



   chorioamnionitis
  

Disease ID 1238
Disease chorioamnionitis
Definition
INFLAMMATION of the placental membranes (CHORION; AMNION) and connected tissues such as fetal BLOOD VESSELS and UMBILICAL CORD. It is often associated with intrauterine ascending infections during PREGNANCY.
Synonym
chorioamnionitides
chorioamnionitis (disorder)
chorioamnionitis [ambiguous]
chorioamnionitis [disease/finding]
membranitis
DOID
UMLS
C0008495
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:26)
C0022876  |  preterm labor  |  6
C0042384  |  vasculitis  |  5
C0007789  |  cerebral palsy  |  4
C0014179  |  uterine infection  |  3
C0000832  |  placental abruption  |  3
C0006287  |  bronchopulmonary dysplasia  |  2
C0022876  |  preterm labour  |  2
C0162429  |  malnutrition  |  1
C0023529  |  periventricular leukomalacia  |  1
C0000832  |  abruptio placentae  |  1
C0004352  |  autism  |  1
C0013418  |  dystocia  |  1
C0032285  |  pulmonary inflammation  |  1
C0032285  |  lung inflammation  |  1
C0022876  |  premature labor  |  1
C0000832  |  abruptio placenta  |  1
C1704437  |  respiratory distress syndrome  |  1
C0011570  |  depression  |  1
C0011847  |  diabetes  |  1
C0011849  |  diabetes mellitus  |  1
C0032046  |  placenta previa  |  1
C0002871  |  anemia  |  1
C0028754  |  obesity  |  1
C0020676  |  hypothyroidism  |  1
C0020538  |  hypertensive disorder  |  1
C0000786  |  miscarriage  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:1)
IL1A  |  3552  |  CTD_human
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:1)
7124  |  TNF  |  infer
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:149)
8993  |  PGLYRP1  |  DISEASES
4826  |  NNAT  |  DISEASES
1943  |  EFNA2  |  DISEASES
5008  |  OSM  |  DISEASES
28231  |  SLCO4A1  |  DISEASES
5020  |  OXT  |  DISEASES
3929  |  LBP  |  DISEASES
7076  |  TIMP1  |  DISEASES
973  |  CD79A  |  DISEASES
6348  |  CCL3  |  DISEASES
4353  |  MPO  |  DISEASES
1440  |  CSF3  |  DISEASES
6347  |  CCL2  |  DISEASES
4790  |  NFKB1  |  DISEASES
3558  |  IL2  |  DISEASES
6688  |  SPI1  |  DISEASES
3458  |  IFNG  |  DISEASES
9450  |  LY86  |  DISEASES
3003  |  GZMK  |  DISEASES
4012  |  LNPEP  |  DISEASES
3565  |  IL4  |  DISEASES
56920  |  SEMA3G  |  DISEASES
3554  |  IL1R1  |  DISEASES
9173  |  IL1RL1  |  DISEASES
4317  |  MMP8  |  DISEASES
4360  |  MRC1  |  DISEASES
5184  |  PEPD  |  DISEASES
54210  |  TREM1  |  DISEASES
652  |  BMP4  |  DISEASES
29108  |  PYCARD  |  DISEASES
968  |  CD68  |  DISEASES
6351  |  CCL4  |  DISEASES
2006  |  ELN  |  DISEASES
10266  |  RAMP2  |  DISEASES
1401  |  CRP  |  DISEASES
3656  |  IRAK2  |  DISEASES
29969  |  MDFIC  |  DISEASES
3569  |  IL6  |  DISEASES
9238  |  TBRG4  |  DISEASES
7097  |  TLR2  |  DISEASES
10728  |  PTGES3  |  DISEASES
3552  |  IL1A  |  DISEASES
3553  |  IL1B  |  DISEASES
1991  |  ELANE  |  DISEASES
3791  |  KDR  |  DISEASES
2255  |  FGF10  |  DISEASES
3383  |  ICAM1  |  DISEASES
54504  |  CPVL  |  DISEASES
3484  |  IGFBP1  |  DISEASES
1392  |  CRH  |  DISEASES
3606  |  IL18  |  DISEASES
5281  |  PIGF  |  DISEASES
54842  |  MFSD6  |  DISEASES
7082  |  TJP1  |  DISEASES
2321  |  FLT1  |  DISEASES
23643  |  LY96  |  DISEASES
11309  |  SLCO2B1  |  DISEASES
873  |  CBR1  |  DISEASES
3101  |  HK3  |  DISEASES
6374  |  CXCL5  |  DISEASES
1672  |  DEFB1  |  DISEASES
1673  |  DEFB4A  |  DISEASES
929  |  CD14  |  DISEASES
3627  |  CXCL10  |  DISEASES
6373  |  CXCL11  |  DISEASES
150684  |  COMMD1  |  DISEASES
3964  |  LGALS8  |  DISEASES
836  |  CASP3  |  DISEASES
348938  |  NIPAL4  |  DISEASES
3642  |  INSM1  |  DISEASES
30835  |  CD209  |  DISEASES
6440  |  SFTPC  |  DISEASES
1442  |  CSH1  |  DISEASES
150696  |  PROM2  |  DISEASES
140596  |  DEFB104A  |  DISEASES
414325  |  DEFB103A  |  DISEASES
503618  |  DEFB104B  |  DISEASES
4312  |  MMP1  |  DISEASES
5021  |  OXTR  |  DISEASES
55894  |  DEFB103B  |  DISEASES
5178  |  PEG3  |  DISEASES
6097  |  RORC  |  DISEASES
4843  |  NOS2  |  DISEASES
1668  |  DEFA3  |  DISEASES
3543  |  IGLL1  |  DISEASES
10732  |  TCFL5  |  DISEASES
7100  |  TLR5  |  DISEASES
6590  |  SLPI  |  DISEASES
3146  |  HMGB1  |  DISEASES
3605  |  IL17A  |  DISEASES
100506658  |  OCLN  |  DISEASES
5284  |  PIGR  |  DISEASES
10219  |  KLRG1  |  DISEASES
7867  |  MAPKAPK3  |  DISEASES
871  |  SERPINH1  |  DISEASES
1524  |  CX3CR1  |  DISEASES
55010  |  PARPBP  |  DISEASES
9332  |  CD163  |  DISEASES
617  |  BCS1L  |  DISEASES
11314  |  CD300A  |  DISEASES
54106  |  TLR9  |  DISEASES
58484  |  NLRC4  |  DISEASES
4283  |  CXCL9  |  DISEASES
7096  |  TLR1  |  DISEASES
440730  |  TRIM67  |  DISEASES
5743  |  PTGS2  |  DISEASES
51744  |  CD244  |  DISEASES
57823  |  SLAMF7  |  DISEASES
6283  |  S100A12  |  DISEASES
5406  |  PNLIP  |  DISEASES
51750  |  RTEL1  |  DISEASES
959  |  CD40LG  |  DISEASES
5737  |  PTGFR  |  DISEASES
81030  |  ZBP1  |  DISEASES
7422  |  VEGFA  |  DISEASES
4318  |  MMP9  |  DISEASES
9670  |  IPO13  |  DISEASES
2022  |  ENG  |  DISEASES
4153  |  MBL2  |  DISEASES
7099  |  TLR4  |  DISEASES
199  |  AIF1  |  DISEASES
50943  |  FOXP3  |  DISEASES
7010  |  TEK  |  DISEASES
3045  |  HBD  |  DISEASES
114131  |  UCN3  |  DISEASES
10333  |  TLR6  |  DISEASES
9037  |  SEMA5A  |  DISEASES
1667  |  DEFA1  |  DISEASES
728358  |  DEFA1B  |  DISEASES
201633  |  TIGIT  |  DISEASES
348801  |  LNP1  |  DISEASES
9467  |  SH3BP5  |  DISEASES
6710  |  SPTB  |  DISEASES
1443  |  CSH2  |  DISEASES
6439  |  SFTPB  |  DISEASES
9560  |  CCL4L2  |  DISEASES
6355  |  CCL8  |  DISEASES
2919  |  CXCL1  |  DISEASES
174  |  AFP  |  DISEASES
837  |  CASP4  |  DISEASES
7124  |  TNF  |  DISEASES
11155  |  LDB3  |  DISEASES
388372  |  CCL4L1  |  DISEASES
79827  |  CLMP  |  DISEASES
3586  |  IL10  |  DISEASES
100289462  |  DEFB4B  |  DISEASES
55331  |  ACER3  |  DISEASES
5228  |  PGF  |  DISEASES
820  |  CAMP  |  DISEASES
Locus(Waiting for update.)
Disease ID 1238
Disease chorioamnionitis
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:27)
HP:0001622  |  Premature delivery  |  15
HP:0001788  |  Premature rupture of membranes  |  12
HP:0100806  |  Sepsis  |  11
HP:0002633  |  Vasculitis  |  5
HP:0100021  |  Cerebral palsy  |  4
HP:0011419  |  Abruptio placentae  |  4
HP:0001511  |  Prenatal onset growth retardation  |  2
HP:0001945  |  Fever  |  2
HP:0040187  |  Neonatal sepsis  |  2
HP:0001510  |  Growth deficiency  |  1
HP:0002045  |  Abnormally low body temperature  |  1
HP:0001513  |  Obesity  |  1
HP:0006970  |  Periventricular leukomalacia  |  1
HP:0001903  |  Anemia  |  1
HP:0004395  |  Malnutrition  |  1
HP:0001263  |  Developmental retardation  |  1
HP:0000470  |  Decreased cervical height  |  1
HP:0001518  |  Small for gestational age  |  1
HP:0000717  |  Autism  |  1
HP:0000819  |  Diabetes mellitus  |  1
HP:0030245  |  Maternal fever during labor  |  1
HP:0000716  |  Depression  |  1
HP:0030009  |  Incompetent cervix  |  1
HP:0001941  |  acidemia  |  1
HP:0000821  |  Underactive thyroid  |  1
HP:0011413  |  Shoulder dystocia  |  1
HP:0002098  |  Respiratory distress  |  1
Disease ID 1238
Disease chorioamnionitis
Manually Symptom(Waiting for update.)
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:5)
C0009450  |  infection  |  15
C1275592  |  funisitis  |  9
C0022876  |  preterm labor  |  6
C0007789  |  cerebral palsy  |  4
C0426768  |  o sign  |  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.)