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Pediatric Disease Annotations & Medicines



   childhood type dermatomyositis
  

Disease ID 1444
Disease childhood type dermatomyositis
Definition
An inflammatory myopathy of childhood resulting in muscle weakness, and associated with a characteristic skin rash.(NICHD)
Synonym
childhood dermatomyositis
childhood type dermatomyositides
childhood type dermatomyositis (disorder)
dermatomyositides, childhood type
dermatomyositis, childhood type
jdm
juvenile dermatomyositis
juvenile dermatomyositis (disorder)
juvenile myositis
Orphanet
DOID
UMLS
C0263666
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:20)
C0006663  |  calcinosis  |  8
C0206062  |  interstitial lung disease  |  5
C0024115  |  lung disease  |  4
C0015230  |  rash  |  1
C0003864  |  arthritis  |  1
C0008325  |  cholecystitis  |  1
C0030326  |  panniculitis  |  1
C0043117  |  immune thrombocytopenic purpura  |  1
C0002878  |  hemolytic anemia  |  1
C0021053  |  immune disease  |  1
C0553662  |  juvenile idiopathic arthritis  |  1
C0006840  |  candidiasis  |  1
C0267841  |  acalculous cholecystitis  |  1
C0008049  |  varicella  |  1
C0206062  |  interstitial lung diseases  |  1
C0024115  |  lung diseases  |  1
C0022398  |  hyperimmunoglobulin e syndrome  |  1
C0008049  |  varicella infection  |  1
C0037274  |  skin disease  |  1
C0002871  |  anemia  |  1
Curated Gene(Waiting for update.)
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:1)
3117  |  HLA-DQA1  |  infer
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:105)
2288  |  FKBP4  |  DISEASES
6362  |  CCL18  |  DISEASES
6347  |  CCL2  |  DISEASES
3381  |  IBSP  |  DISEASES
969  |  CD69  |  DISEASES
4256  |  MGP  |  DISEASES
23438  |  HARS2  |  DISEASES
6678  |  SPARC  |  DISEASES
6431  |  SRSF6  |  DISEASES
5184  |  PEPD  |  DISEASES
6631  |  SNRPC  |  DISEASES
57505  |  AARS2  |  DISEASES
3232  |  HOXD3  |  DISEASES
6737  |  TRIM21  |  DISEASES
3569  |  IL6  |  DISEASES
640  |  BLK  |  DISEASES
55014  |  STX17  |  DISEASES
6366  |  CCL21  |  DISEASES
7057  |  THBS1  |  DISEASES
7450  |  VWF  |  DISEASES
16  |  AARS  |  DISEASES
9172  |  MYOM2  |  DISEASES
64135  |  IFIH1  |  DISEASES
3299  |  HSF4  |  DISEASES
10190  |  TXNDC9  |  DISEASES
59067  |  IL21  |  DISEASES
4437  |  MSH3  |  DISEASES
27074  |  LAMP3  |  DISEASES
5286  |  PIK3C2A  |  DISEASES
3687  |  ITGAX  |  DISEASES
10055  |  SAE1  |  DISEASES
3439  |  IFNA1  |  DISEASES
3606  |  IL18  |  DISEASES
643  |  CXCR5  |  DISEASES
7412  |  VCAM1  |  DISEASES
2215  |  FCGR3B  |  DISEASES
7098  |  TLR3  |  DISEASES
27242  |  TNFRSF21  |  DISEASES
4982  |  TNFRSF11B  |  DISEASES
4054  |  LTBP3  |  DISEASES
6356  |  CCL11  |  DISEASES
3233  |  HOXD4  |  DISEASES
3627  |  CXCL10  |  DISEASES
6363  |  CCL19  |  DISEASES
1776  |  DNASE1L3  |  DISEASES
23129  |  PLXND1  |  DISEASES
4684  |  NCAM1  |  DISEASES
8834  |  TMEM11  |  DISEASES
3563  |  IL3RA  |  DISEASES
3665  |  IRF7  |  DISEASES
60529  |  ALX4  |  DISEASES
3117  |  HLA-DQA1  |  DISEASES
7060  |  THBS4  |  DISEASES
8805  |  TRIM24  |  DISEASES
9218  |  VAPA  |  DISEASES
27030  |  MLH3  |  DISEASES
51592  |  TRIM33  |  DISEASES
3123  |  HLA-DRB1  |  DISEASES
127343  |  DMBX1  |  DISEASES
170482  |  CLEC4C  |  DISEASES
56955  |  MEPE  |  DISEASES
1756  |  DMD  |  DISEASES
3211  |  HOXB1  |  DISEASES
23345  |  SYNE1  |  DISEASES
6738  |  TROVE2  |  DISEASES
2214  |  FCGR3A  |  DISEASES
4580  |  MTX1  |  DISEASES
4582  |  MUC1  |  DISEASES
6283  |  S100A12  |  DISEASES
2018  |  EMX2  |  DISEASES
959  |  CD40LG  |  DISEASES
3437  |  IFIT3  |  DISEASES
1503  |  CTPS1  |  DISEASES
64102  |  TNMD  |  DISEASES
3108  |  HLA-DMA  |  DISEASES
5698  |  PSMB9  |  DISEASES
3118  |  HLA-DQA2  |  DISEASES
10673  |  TNFSF13B  |  DISEASES
50943  |  FOXP3  |  DISEASES
7133  |  TNFRSF1B  |  DISEASES
1041  |  CDSN  |  DISEASES
5394  |  EXOSC10  |  DISEASES
8718  |  TNFRSF25  |  DISEASES
57623  |  ZFAT  |  DISEASES
441376  |  AARD  |  DISEASES
4897  |  NRCAM  |  DISEASES
9636  |  ISG15  |  DISEASES
11168  |  PSIP1  |  DISEASES
2591  |  GALNT3  |  DISEASES
6696  |  SPP1  |  DISEASES
3965  |  LGALS9  |  DISEASES
4599  |  MX1  |  DISEASES
23515  |  MORC3  |  DISEASES
197  |  AHSG  |  DISEASES
720  |  C4A  |  DISEASES
7124  |  TNF  |  DISEASES
5334  |  PLCL1  |  DISEASES
3609  |  ILF3  |  DISEASES
3115  |  HLA-DPB1  |  DISEASES
721  |  C4B  |  DISEASES
3035  |  HARS  |  DISEASES
114907  |  FBXO32  |  DISEASES
930  |  CD19  |  DISEASES
3227  |  HOXC11  |  DISEASES
6625  |  SNRNP70  |  DISEASES
Locus(Waiting for update.)
Disease ID 1444
Disease childhood type dermatomyositis
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:11)
HP:0003761  |  Calcinosis  |  7
HP:0006530  |  Interstitial lung disease  |  5
HP:0000969  |  Dropsy  |  2
HP:0002960  |  Autoimmune condition  |  1
HP:0005681  |  Juvenile idiopathic arthritis  |  1
HP:0001903  |  Anemia  |  1
HP:0012490  |  Inflammation of fat tissue  |  1
HP:0001878  |  Haemolytic anaemia  |  1
HP:0007430  |  Generalized edema  |  1
HP:0001082  |  Cholecystitis  |  1
HP:0001369  |  Arthritis  |  1
Disease ID 1444
Disease childhood type dermatomyositis
Manually Symptom(Waiting for update.)
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:4)
C0006663  |  calcinosis  |  7
C0206062  |  interstitial lung disease  |  5
C0015230  |  rash  |  1
C0030326  |  panniculitis  |  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.)