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Pediatric Disease Annotations & Medicines



   pyoderma
  

Disease ID 1479
Disease pyoderma
Definition
Any purulent skin disease (Dorland, 27th ed).
Synonym
dermatitis pyogenic
dermatitis, purulent
dermatitis, septic
dermatitis, suppurative
purulent dermatitis
pus-filled lesion
pyoderma (disorder)
pyoderma (skin infection)
pyoderma [disease/finding]
pyoderma nos
pyoderma nos (disorder)
pyoderma, unspecified
pyodermas
pyodermia
pyogenic dermatitis
pyogenic infection of skin and subcutis
septic dermatitis
suppurative dermatitis
DOID
ICD10
UMLS
C0034212
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:59)
C0009324  |  ulcerative colitis  |  15
C0021831  |  bowel disease  |  10
C0021390  |  inflammatory bowel disease  |  10
C0009319  |  colitis  |  8
C0010346  |  crohn's disease  |  7
C0036416  |  scleritis  |  2
C0042384  |  vasculitis  |  2
C0026986  |  myelodysplastic syndrome  |  2
C0007102  |  colon cancer  |  2
C0206693  |  medullary carcinoma  |  1
C0003864  |  arthritis  |  1
C0019158  |  hepatitis  |  1
C0241910  |  autoimmune hepatitis  |  1
C0152026  |  retinal vasculitis  |  1
C0002726  |  amyloidosis  |  1
C0030312  |  pancytopenia  |  1
C0007570  |  celiac disease  |  1
C0263398  |  erythema elevatum diutinum  |  1
C0029443  |  osteomyelitis  |  1
C1704437  |  respiratory distress syndrome  |  1
C0027947  |  neutropenia  |  1
C0221026  |  x-linked agammaglobulinemia  |  1
C0021171  |  incontinentia pigmenti  |  1
C0042769  |  viral infection  |  1
C0410422  |  chronic recurrent multifocal osteomyelitis  |  1
C0012814  |  colonic diverticulitis  |  1
C0004903  |  beckwith wiedemann syndrome  |  1
C0001768  |  agammaglobulinemia  |  1
C0281963  |  red cell aplasia  |  1
C0162836  |  hidradenitis suppurativa  |  1
C0036421  |  systemic sclerosis  |  1
C0085160  |  hidradenitis  |  1
C0036262  |  scabies  |  1
C0026764  |  myeloma  |  1
C0079774  |  peripheral t-cell lymphoma  |  1
C0024314  |  lymphoproliferative disorder  |  1
C0009447  |  common variable immunodeficiency  |  1
C0001815  |  chronic idiopathic myelofibrosis  |  1
C0221023  |  cyclic neutropenia  |  1
C0030807  |  pemphigus  |  1
C0004623  |  bacterial infection  |  1
C0039263  |  takayasu's arteritis  |  1
C0238462  |  medullary carcinoma of the thyroid  |  1
C0035222  |  acute respiratory distress syndrome  |  1
C0022568  |  keratitis  |  1
C0019196  |  hepatitis c  |  1
C0001815  |  idiopathic myelofibrosis  |  1
C0042769  |  virus infection  |  1
C1692886  |  pyogenic arthritis  |  1
C0003873  |  rheumatoid arthritis  |  1
C0276758  |  fusarium infection  |  1
C0001815  |  myelofibrosis  |  1
C0011603  |  dermatitis  |  1
C0272412  |  splenic abscess  |  1
C0030809  |  pemphigus vulgaris  |  1
C0007134  |  renal carcinoma  |  1
C0034902  |  pure red cell aplasia  |  1
C0012813  |  diverticulitis  |  1
C0376545  |  hematological malignancy  |  1
Curated Gene(Waiting for update.)
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:134)
1015  |  CDH17  |  DISEASES
7132  |  TNFRSF1A  |  DISEASES
26469  |  PTPN18  |  DISEASES
80863  |  PRRT1  |  DISEASES
4210  |  MEFV  |  DISEASES
973  |  CD79A  |  DISEASES
4353  |  MPO  |  DISEASES
1440  |  CSF3  |  DISEASES
1075  |  CTSC  |  DISEASES
4598  |  MVK  |  DISEASES
3273  |  HRG  |  DISEASES
566  |  AZU1  |  DISEASES
5657  |  PRTN3  |  DISEASES
5266  |  PI3  |  DISEASES
667  |  DST  |  DISEASES
5782  |  PTPN12  |  DISEASES
7263  |  TST  |  DISEASES
79733  |  E2F8  |  DISEASES
4695  |  NDUFA2  |  DISEASES
1401  |  CRP  |  DISEASES
10955  |  SERINC3  |  DISEASES
1830  |  DSG3  |  DISEASES
1828  |  DSG1  |  DISEASES
1823  |  DSC1  |  DISEASES
9958  |  USP15  |  DISEASES
3569  |  IL6  |  DISEASES
3557  |  IL1RN  |  DISEASES
27179  |  IL36A  |  DISEASES
26525  |  IL36RN  |  DISEASES
971  |  CD72  |  DISEASES
3795  |  KHK  |  DISEASES
1829  |  DSG2  |  DISEASES
9663  |  LPIN2  |  DISEASES
23184  |  MESDC2  |  DISEASES
9172  |  MYOM2  |  DISEASES
7011  |  TEP1  |  DISEASES
23523  |  CABIN1  |  DISEASES
8424  |  BBOX1  |  DISEASES
4924  |  NUCB1  |  DISEASES
3553  |  IL1B  |  DISEASES
9410  |  SNRNP40  |  DISEASES
943  |  TNFRSF8  |  DISEASES
3299  |  HSF4  |  DISEASES
59274  |  MESDC1  |  DISEASES
3858  |  KRT10  |  DISEASES
3606  |  IL18  |  DISEASES
26040  |  SETBP1  |  DISEASES
220134  |  SKA1  |  DISEASES
653361  |  NCF1  |  DISEASES
58191  |  CXCL16  |  DISEASES
23385  |  NCSTN  |  DISEASES
7203  |  CCT3  |  DISEASES
327  |  APEH  |  DISEASES
3562  |  IL3  |  DISEASES
1437  |  CSF2  |  DISEASES
6862  |  T  |  DISEASES
79841  |  AGBL2  |  DISEASES
717  |  C2  |  DISEASES
5896  |  RAG1  |  DISEASES
22974  |  TPX2  |  DISEASES
64127  |  NOD2  |  DISEASES
56547  |  MMP26  |  DISEASES
55630  |  SLC39A4  |  DISEASES
3868  |  KRT16  |  DISEASES
116071  |  BATF2  |  DISEASES
84168  |  ANTXR1  |  DISEASES
3689  |  ITGB2  |  DISEASES
29  |  ABR  |  DISEASES
9655  |  SOCS5  |  DISEASES
8436  |  SDPR  |  DISEASES
118429  |  ANTXR2  |  DISEASES
56246  |  MRAP  |  DISEASES
3913  |  LAMB2  |  DISEASES
121391  |  KRT74  |  DISEASES
695  |  BTK  |  DISEASES
155465  |  AGR3  |  DISEASES
9986  |  RCE1  |  DISEASES
56776  |  FMN2  |  DISEASES
91662  |  NLRP12  |  DISEASES
2193  |  FARSA  |  DISEASES
9322  |  TRIP10  |  DISEASES
199699  |  DAND5  |  DISEASES
147719  |  LYPD4  |  DISEASES
5155  |  PDGFB  |  DISEASES
2242  |  FES  |  DISEASES
348235  |  SKA2  |  DISEASES
114548  |  NLRP3  |  DISEASES
1308  |  COL17A1  |  DISEASES
5275  |  SERPINB13  |  DISEASES
25870  |  SUMF2  |  DISEASES
3605  |  IL17A  |  DISEASES
79092  |  CARD14  |  DISEASES
3638  |  INSIG1  |  DISEASES
23764  |  MAFF  |  DISEASES
3683  |  ITGAL  |  DISEASES
83658  |  DYNLRB1  |  DISEASES
23556  |  PIGN  |  DISEASES
3635  |  INPP5D  |  DISEASES
147409  |  DSG4  |  DISEASES
3164  |  NR4A1  |  DISEASES
58484  |  NLRC4  |  DISEASES
9760  |  TOX  |  DISEASES
1380  |  CR2  |  DISEASES
10758  |  TRAF3IP2  |  DISEASES
7272  |  TTK  |  DISEASES
2316  |  FLNA  |  DISEASES
8804  |  CREG1  |  DISEASES
959  |  CD40LG  |  DISEASES
729238  |  SFTPA2  |  DISEASES
55315  |  SLC29A3  |  DISEASES
7133  |  TNFRSF1B  |  DISEASES
4524  |  MTHFR  |  DISEASES
1676  |  DFFA  |  DISEASES
1910  |  EDNRB  |  DISEASES
54790  |  TET2  |  DISEASES
51109  |  RDH11  |  DISEASES
22900  |  CARD8  |  DISEASES
347734  |  SLC35B2  |  DISEASES
23077  |  MYCBP2  |  DISEASES
9050  |  PSTPIP2  |  DISEASES
10551  |  AGR2  |  DISEASES
5777  |  PTPN6  |  DISEASES
7124  |  TNF  |  DISEASES
6635  |  SNRPE  |  DISEASES
23098  |  SARM1  |  DISEASES
6358  |  CCL14  |  DISEASES
834  |  CASP1  |  DISEASES
721  |  C4B  |  DISEASES
8801  |  SUCLG2  |  DISEASES
83695  |  RHNO1  |  DISEASES
9051  |  PSTPIP1  |  DISEASES
22861  |  NLRP1  |  DISEASES
79104  |  MEG8  |  DISEASES
100128252  |  ZNF667-AS1  |  DISEASES
Locus(Waiting for update.)
Disease ID 1479
Disease pyoderma
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:35)
HP:0100279  |  Ulcerative colitis  |  14
HP:0002583  |  Colitis  |  7
HP:0100280  |  Morbus Crohn  |  7
HP:0002863  |  Myelodysplastic syndrome  |  2
HP:0003003  |  Colon cancer  |  2
HP:0100532  |  Scleritis  |  2
HP:0002633  |  Vasculitis  |  2
HP:0004432  |  Agammaglobulinaemia  |  1
HP:0002955  |  Granulomatosis  |  1
HP:0040154  |  Hidradenitis suppurativa  |  1
HP:0001762  |  Talipes equinovarus  |  1
HP:0005584  |  Renal cell carcinoma  |  1
HP:0012115  |  Liver inflammation  |  1
HP:0002608  |  Celiac disease  |  1
HP:0011974  |  Myelofibrosis  |  1
HP:0005901  |  Chronic recurrent multifocal osteomyelitis  |  1
HP:0100583  |  Corneal perforation  |  1
HP:0011034  |  Amyloid disease  |  1
HP:0000491  |  Corneal inflammation  |  1
HP:0001875  |  Neutropenia  |  1
HP:0003270  |  Distended abdomen  |  1
HP:0100550  |  Rupture of tendons  |  1
HP:0100847  |  Pustulosis palmaris et plantaris  |  1
HP:0000155  |  Oral ulcer  |  1
HP:0012410  |  Pure red cell aplasia  |  1
HP:0200042  |  Skin ulcer  |  1
HP:0002098  |  Respiratory distress  |  1
HP:0005523  |  Lymphoproliferative disorder  |  1
HP:0012089  |  Arteritis  |  1
HP:0010783  |  Erythema  |  1
HP:0001876  |  Low blood cell count  |  1
HP:0008110  |  Equinovarus deformity  |  1
HP:0002754  |  Bone infection  |  1
HP:0001370  |  Rheumatoid arthritis  |  1
HP:0001369  |  Arthritis  |  1
Disease ID 1479
Disease pyoderma
Manually Symptom(Waiting for update.)
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:1)
C0037284  |  skin lesions  |  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.)