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Pediatric Disease Annotations & Medicines



   cytomegalovirus retinitis
  

Disease ID 781
Disease cytomegalovirus retinitis
Definition
Infection of the retina by cytomegalovirus characterized by retinal necrosis, hemorrhage, vessel sheathing, and retinal edema. Cytomegalovirus retinitis is a major opportunistic infection in AIDS patients and can cause blindness.
Synonym
cmv - cytomegalovirus retinitis
cmv retinitis
cytomegaloviral retinitis
cytomegaloviral retinitis (disorder)
cytomegalovirus retinitis [disease/finding]
retinitis cmv
retinitis, cytomegaloviral
retinitis, cytomegalovirus
UMLS
C0206178
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:22)
C0001175  |  acquired immunodeficiency syndrome  |  6
C0020538  |  hypertension  |  1
C0001175  |  acquired immune deficiency syndrome  |  1
C0032285  |  pneumonia  |  1
C0035305  |  retinal detachment  |  1
C0011847  |  diabetes  |  1
C0019829  |  hodgkin's lymphoma  |  1
C0036220  |  kaposi's sarcoma  |  1
C0036454  |  visual field loss  |  1
C0026764  |  multiple myeloma  |  1
C0001175  |  acquired immunodeficiency syndrome (aids)  |  1
C0029134  |  optic neuritis  |  1
C0028242  |  nocardiosis  |  1
C0027813  |  neuritis  |  1
C0024440  |  cystoid macular edema  |  1
C0086543  |  cataract  |  1
C0024305  |  non-hodgkin's lymphoma  |  1
C0001175  |  acquired immune deficiency  |  1
C0221027  |  good's syndrome  |  1
C0042164  |  uveitis  |  1
C0456909  |  blindness  |  1
C0043092  |  wegener's granulomatosis  |  1
Curated Gene(Waiting for update.)
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:74)
6376  |  CX3CL1  |  DISEASES
920  |  CD4  |  DISEASES
11035  |  RIPK3  |  DISEASES
7036  |  TFR2  |  DISEASES
1440  |  CSF3  |  DISEASES
6347  |  CCL2  |  DISEASES
3558  |  IL2  |  DISEASES
3587  |  IL10RA  |  DISEASES
3458  |  IFNG  |  DISEASES
5967  |  REG1A  |  DISEASES
5657  |  PRTN3  |  DISEASES
84329  |  HVCN1  |  DISEASES
7389  |  UROD  |  DISEASES
2670  |  GFAP  |  DISEASES
6538  |  SLC6A11  |  DISEASES
2995  |  GYPC  |  DISEASES
8737  |  RIPK1  |  DISEASES
4069  |  LYZ  |  DISEASES
6121  |  RPE65  |  DISEASES
55850  |  USE1  |  DISEASES
943  |  TNFRSF8  |  DISEASES
7297  |  TYK2  |  DISEASES
939  |  CD27  |  DISEASES
3930  |  LBR  |  DISEASES
6529  |  SLC6A1  |  DISEASES
8566  |  PDXK  |  DISEASES
729230  |  CCR2  |  DISEASES
1234  |  CCR5  |  DISEASES
6352  |  CCL5  |  DISEASES
3577  |  CXCR1  |  DISEASES
9607  |  CARTPT  |  DISEASES
1437  |  CSF2  |  DISEASES
9655  |  SOCS5  |  DISEASES
3627  |  CXCL10  |  DISEASES
56246  |  MRAP  |  DISEASES
27289  |  RND1  |  DISEASES
947  |  CD34  |  DISEASES
8884  |  SLC5A6  |  DISEASES
27243  |  CHMP2A  |  DISEASES
8651  |  SOCS1  |  DISEASES
148738  |  HFE2  |  DISEASES
9094  |  UNC119  |  DISEASES
1908  |  EDN3  |  DISEASES
6540  |  SLC6A13  |  DISEASES
4942  |  OAT  |  DISEASES
153  |  ADRB1  |  DISEASES
959  |  CD40LG  |  DISEASES
1025  |  CDK9  |  DISEASES
3376  |  IARS  |  DISEASES
6564  |  SLC15A1  |  DISEASES
3105  |  HLA-A  |  DISEASES
2550  |  GABBR1  |  DISEASES
6354  |  CCL7  |  DISEASES
4038  |  LRP4  |  DISEASES
375790  |  AGRN  |  DISEASES
6152  |  RPL24  |  DISEASES
3119  |  HLA-DQB1  |  DISEASES
3120  |  HLA-DQB2  |  DISEASES
5076  |  PAX2  |  DISEASES
7124  |  TNF  |  DISEASES
3106  |  HLA-B  |  DISEASES
7072  |  TIA1  |  DISEASES
4049  |  LTA  |  DISEASES
81704  |  DOCK8  |  DISEASES
1154  |  CISH  |  DISEASES
4050  |  LTB  |  DISEASES
3586  |  IL10  |  DISEASES
100506742  |  CASP12  |  DISEASES
83695  |  RHNO1  |  DISEASES
1232  |  CCR3  |  DISEASES
80184  |  CEP290  |  DISEASES
10381  |  TUBB3  |  DISEASES
56963  |  RGMA  |  DISEASES
2323  |  FLT3LG  |  DISEASES
Locus(Waiting for update.)
Disease ID 781
Disease cytomegalovirus retinitis
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:17)
HP:0002721  |  Immunodeficiency  |  7
HP:0000518  |  Cataract  |  1
HP:0011505  |  Cystoid macular edema  |  1
HP:0012089  |  Arteritis  |  1
HP:0000541  |  Detached retina  |  1
HP:0006775  |  Multiple myeloma  |  1
HP:0012189  |  Hodgkin disease  |  1
HP:0000822  |  Hypertension  |  1
HP:0002090  |  Pneumonia  |  1
HP:0000554  |  Uveitis  |  1
HP:0000505  |  Poor vision  |  1
HP:0100653  |  Optic neuritis  |  1
HP:0007985  |  Retinal arteriolar occlusion  |  1
HP:0100726  |  Kaposi's sarcoma  |  1
HP:0007902  |  Vitreous hemorrhage  |  1
HP:0000572  |  Visual loss  |  1
HP:0000618  |  Blindness  |  1
Disease ID 781
Disease cytomegalovirus retinitis
Manually Symptom
UMLS  | Name(Total Manually Symptoms:13)
C1963266  |  uveitis
C1963229  |  retinal detachment
C1532529  |  frosted branch angiitis
C0456909  |  vision loss
C0426768  |  o sign
C0235812  |  vitritis
C0221027  |  good's syndrome
C0035321  |  retinal tears
C0035305  |  retinal detachments
C0031129  |  periphlebitis
C0028841  |  ocular hypotony
C0024440  |  cystoid macular edema
C0019080  |  hemorrhage
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:5)
C0019080  |  hemorrhage  |  1
C0035305  |  retinal detachment  |  1
C0042164  |  uveitis  |  1
C0024440  |  cystoid macular edema  |  1
C0221027  |  good's syndrome  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:3)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs2228055206179243587IL10RAumls:C0206178BeFreeIn European Americans (n = 750), a haplotype carrying an amino acid changing variation in the cytoplasmic domain (S420L) of IL-10R1 can be protective (OR, 0.14; 95% CI, 0.02-0.94; P = .04) against, whereas another haplotype carrying an amino acid changing variation in the extracellular domain (I224V) of IL-10R1 can be more susceptible (OR, 6.21; 95% CI, 1.22- 31.54; P = .03) to CMV retinitis.0.0026384742010IL10RA11117994131AG
rs2229114206179243587IL10RAumls:C0206178BeFreeIn European Americans (n = 750), a haplotype carrying an amino acid changing variation in the cytoplasmic domain (S420L) of IL-10R1 can be protective (OR, 0.14; 95% CI, 0.02-0.94; P = .04) against, whereas another haplotype carrying an amino acid changing variation in the extracellular domain (I224V) of IL-10R1 can be more susceptible (OR, 6.21; 95% CI, 1.22- 31.54; P = .03) to CMV retinitis.0.0026384742010IL10RA11117999163CT
rs386479044206179243587IL10RAumls:C0206178BeFreeIn European Americans (n = 750), a haplotype carrying an amino acid changing variation in the cytoplasmic domain (S420L) of IL-10R1 can be protective (OR, 0.14; 95% CI, 0.02-0.94; P = .04) against, whereas another haplotype carrying an amino acid changing variation in the extracellular domain (I224V) of IL-10R1 can be more susceptible (OR, 6.21; 95% CI, 1.22- 31.54; P = .03) to CMV retinitis.0.0026384742010NANANANANA
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:4)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0206178cidofovirC059262113852-37-2cytomegalovirus retinitisMESH:D017726therapeutic9525435
C0206178cyclophosphamideD00352050-18-0cytomegalovirus retinitisMESH:D017726marker/mechanism12488280
C0206178foscarnetD0172454428-95-9cytomegalovirus retinitisMESH:D017726therapeutic11363124
C0206178ganciclovirD01577482410-32-0cytomegalovirus retinitisMESH:D017726therapeutic11363124
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)