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Pediatric Disease Annotations & Medicines



   dermatomyositis
  

Disease ID 66
Disease dermatomyositis
Definition
A subacute or chronic inflammatory disease of muscle and skin, marked by proximal muscle weakness and a characteristic skin rash. The illness occurs with approximately equal frequency in children and adults. The skin lesions usually take the form of a purplish rash (or less often an exfoliative dermatitis) involving the nose, cheeks, forehead, upper trunk, and arms. The disease is associated with a complement mediated intramuscular microangiopathy, leading to loss of capillaries, muscle ischemia, muscle-fiber necrosis, and perifascicular atrophy. The childhood form of this disease tends to evolve into a systemic vasculitis. Dermatomyositis may occur in association with malignant neoplasms. (From Adams et al., Principles of Neurology, 6th ed, pp1405-6)
Synonym
[x]dermatopolymyositis, unspecified
[x]dermatopolymyositis, unspecified (disorder)
dermatomucosomyositis
dermatomyositides
dermatomyositis (disorder)
dermatomyositis [disease/finding]
dermatopolymyositides
dermatopolymyositis
dm - dermatomyositis
polymyositis dermatomyositis
polymyositis with skin involvement
polymyositis-dermatomyositides
polymyositis-dermatomyositis
polymyositis/dermatomyositis
wagner-unverricht syndrome
Orphanet
DOID
UMLS
C0011633
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:127)
C0206062  |  interstitial lung disease  |  27
C0024115  |  lung disease  |  23
C0032285  |  pneumonia  |  10
C0006663  |  calcinosis  |  9
C0003864  |  arthritis  |  5
C0003873  |  rheumatoid arthritis  |  5
C0042384  |  vasculitis  |  4
C0238301  |  nasopharyngeal carcinoma  |  4
C0030326  |  panniculitis  |  3
C0015230  |  rash  |  3
C0006142  |  breast cancer  |  3
C0085655  |  polymyositis  |  3
C0019158  |  hepatitis  |  2
C0699885  |  bladder carcinoma  |  2
C0684249  |  carcinoma of the lung  |  2
C0153452  |  gallbladder ca  |  2
C0235618  |  proliferative glomerulonephritis  |  2
C0235782  |  gallbladder carcinoma  |  2
C0001418  |  adenocarcinoma  |  2
C0039590  |  testicular cancer  |  2
C0206062  |  interstitial lung diseases  |  2
C0024115  |  lung diseases  |  2
C0027121  |  myositis  |  2
C0011644  |  scleroderma  |  2
C0025202  |  melanoma  |  2
C0242379  |  lung cancer  |  2
C1279945  |  acute interstitial pneumonia  |  2
C0017662  |  membranoproliferative glomerulonephritis  |  1
C0677607  |  hashimoto thyroiditis  |  1
C0948265  |  metabolic syndrome  |  1
C0042109  |  urticarial  |  1
C1261473  |  soft tissue sarcoma  |  1
C0023787  |  lipodystrophy  |  1
C0032027  |  pityriasis rubra pilaris  |  1
C0238463  |  papillary thyroid cancer  |  1
C0302592  |  carcinoma of cervix  |  1
C0040034  |  thrombocytopenia  |  1
C0005684  |  bladder cancer  |  1
C0038358  |  gastric ulcer  |  1
C0032305  |  pneumocystis  |  1
C0038358  |  gastric ulcers  |  1
C0031347  |  pharyngeal cancer  |  1
C0235025  |  motor neuropathy  |  1
C1253936  |  joint effusion  |  1
C0011991  |  diarrhea  |  1
C0007570  |  celiac disease  |  1
C0039538  |  teratoma  |  1
C0019360  |  herpes zoster  |  1
C1333977  |  hepatitis b virus-related hepatocellular carcinoma  |  1
C0009326  |  collagen disease  |  1
C0241910  |  autoimmune hepatitis  |  1
C0037274  |  dermatosis  |  1
C0017658  |  glomerulonephritis  |  1
C0009782  |  connective tissue disease  |  1
C0032131  |  plasmacytoma  |  1
C1527407  |  eosinophilic pneumonia  |  1
C0153392  |  nasopharyngeal cancer  |  1
C0085253  |  adult-onset still's disease  |  1
C0476089  |  endometrial cancer  |  1
C0024225  |  lymphangitis  |  1
C0034069  |  pulmonary fibrosis  |  1
C0409974  |  lupus erythematosus  |  1
C0021053  |  immune disorders  |  1
C0019360  |  zoster  |  1
C1140680  |  ovarian cancer  |  1
C0085278  |  antiphospholipid syndrome  |  1
C0014121  |  infective endocarditis  |  1
C0001144  |  acne vulgaris  |  1
C0007104  |  carcinoma of the breast  |  1
C0040558  |  toxoplasmosis  |  1
C1327709  |  rectosigmoid carcinoma  |  1
C0043117  |  immune thrombocytopenic purpura  |  1
C0022398  |  hyperimmunoglobulin e syndrome  |  1
C0149925  |  small cell lung cancer  |  1
C0007137  |  squamous cell carcinoma  |  1
C0278619  |  extramedullary plasmacytoma  |  1
C0009319  |  colitis  |  1
C0019163  |  hepatitis b  |  1
C0023895  |  liver disease  |  1
C0085278  |  anti-phospholipid syndrome  |  1
C0036421  |  systemic sclerosis  |  1
C0553662  |  juvenile idiopathic arthritis  |  1
C0021053  |  immune disorder  |  1
C0004030  |  aspergillosis  |  1
C0278883  |  metastatic melanoma  |  1
C0558355  |  tonsillar carcinoma  |  1
C0023470  |  myelocytic leukemia  |  1
C0024623  |  gastric cancer  |  1
C0040147  |  thyroiditis  |  1
C0035309  |  retinopathy  |  1
C0034069  |  lung fibrosis  |  1
C1527336  |  sjogren's syndrome  |  1
C0311284  |  multicentric reticulohistiocytosis  |  1
C0014118  |  endocarditis  |  1
C0008049  |  varicella  |  1
C0206698  |  cholangiocarcinoma  |  1
C0280131  |  ovarian teratoma  |  1
C0007115  |  thyroid ca  |  1
C0024141  |  systemic lupus erythematosus  |  1
C0023467  |  acute myelocytic leukemia  |  1
C0920350  |  autoimmune thyroiditis  |  1
C0042384  |  angiitis  |  1
C1266128  |  ossifying fibromyxoid tumor  |  1
C0042769  |  virus infection  |  1
C0149925  |  small cell carcinoma  |  1
C0476089  |  endometrial ca  |  1
C0009326  |  collagen diseases  |  1
C0007115  |  thyroid cancer  |  1
C0152026  |  retinal vasculitis  |  1
C0026848  |  muscle disease  |  1
C0024115  |  pulmonary disorders  |  1
C0152013  |  adenocarcinoma of the lung  |  1
C0024299  |  lymphoma  |  1
C0027873  |  devic's disease  |  1
C0302592  |  carcinoma cervix  |  1
C0026986  |  myelodysplastic syndrome  |  1
C0026896  |  myasthenia gravis  |  1
C1140680  |  ovarian ca  |  1
C0026848  |  myopathies  |  1
C0155765  |  microangiopathy  |  1
C0037274  |  skin disease  |  1
C0008049  |  varicella infection  |  1
C0007102  |  colon cancer  |  1
C0022672  |  acute tubular necrosis  |  1
C0149925  |  small cell carcinoma of the lung  |  1
C0027121  |  inflammatory myopathies  |  1
C0009324  |  ulcerative colitis  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:6)
TNF  |  7124  |  CTD_human
C9  |  735  |  CTD_human
IL1B  |  3553  |  CTD_human
HLA-B  |  3106  |  CTD_human
C2  |  717  |  CTD_human
IL1A  |  3552  |  CTD_human
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:6)
3117  |  HLA-DQA1  |  infer
3123  |  HLA-DRB1  |  infer
3586  |  IL10  |  infer
3552  |  IL1A  |  infer
3553  |  IL1B  |  infer
7124  |  TNF  |  infer
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:271)
6362  |  CCL18  |  DISEASES
6376  |  CX3CL1  |  DISEASES
266  |  AMELY  |  DISEASES
11274  |  USP18  |  DISEASES
6948  |  TCN2  |  DISEASES
84844  |  PHF5A  |  DISEASES
3002  |  GZMB  |  DISEASES
6880  |  TAF9  |  DISEASES
6361  |  CCL17  |  DISEASES
8797  |  TNFRSF10A  |  DISEASES
1158  |  CKM  |  DISEASES
7040  |  TGFB1  |  DISEASES
973  |  CD79A  |  DISEASES
6119  |  RPA3  |  DISEASES
6348  |  CCL3  |  DISEASES
4353  |  MPO  |  DISEASES
6347  |  CCL2  |  DISEASES
3558  |  IL2  |  DISEASES
969  |  CD69  |  DISEASES
4256  |  MGP  |  DISEASES
3458  |  IFNG  |  DISEASES
23517  |  SKIV2L2  |  DISEASES
23438  |  HARS2  |  DISEASES
3565  |  IL4  |  DISEASES
6301  |  SARS  |  DISEASES
84618  |  NT5C1A  |  DISEASES
8161  |  COIL  |  DISEASES
6431  |  SRSF6  |  DISEASES
5184  |  PEPD  |  DISEASES
6631  |  SNRPC  |  DISEASES
57505  |  AARS2  |  DISEASES
718  |  C3  |  DISEASES
1236  |  CCR7  |  DISEASES
85359  |  DGCR6L  |  DISEASES
3232  |  HOXD3  |  DISEASES
4654  |  MYOD1  |  DISEASES
968  |  CD68  |  DISEASES
6351  |  CCL4  |  DISEASES
10155  |  TRIM28  |  DISEASES
22856  |  CHSY1  |  DISEASES
6737  |  TRIM21  |  DISEASES
6117  |  RPA1  |  DISEASES
1401  |  CRP  |  DISEASES
4064  |  CD180  |  DISEASES
10752  |  CHL1  |  DISEASES
4677  |  NARS  |  DISEASES
8728  |  ADAM19  |  DISEASES
3569  |  IL6  |  DISEASES
640  |  BLK  |  DISEASES
55014  |  STX17  |  DISEASES
6366  |  CCL21  |  DISEASES
7057  |  THBS1  |  DISEASES
6741  |  SSB  |  DISEASES
7450  |  VWF  |  DISEASES
16  |  AARS  |  DISEASES
64377  |  CHST8  |  DISEASES
23523  |  CABIN1  |  DISEASES
3552  |  IL1A  |  DISEASES
3553  |  IL1B  |  DISEASES
64135  |  IFIH1  |  DISEASES
9066  |  SYT7  |  DISEASES
51192  |  CKLF  |  DISEASES
941  |  CD80  |  DISEASES
51191  |  HERC5  |  DISEASES
5443  |  POMC  |  DISEASES
3383  |  ICAM1  |  DISEASES
6897  |  TARS  |  DISEASES
27074  |  LAMP3  |  DISEASES
6595  |  SMARCA2  |  DISEASES
5286  |  PIK3C2A  |  DISEASES
80349  |  WDR61  |  DISEASES
10055  |  SAE1  |  DISEASES
3439  |  IFNA1  |  DISEASES
3606  |  IL18  |  DISEASES
79731  |  NARS2  |  DISEASES
925  |  CD8A  |  DISEASES
83648  |  FAM167A  |  DISEASES
351  |  APP  |  DISEASES
10563  |  CXCL13  |  DISEASES
3156  |  HMGCR  |  DISEASES
6294  |  SAFB  |  DISEASES
643  |  CXCR5  |  DISEASES
1234  |  CCR5  |  DISEASES
6368  |  CCL23  |  DISEASES
7412  |  VCAM1  |  DISEASES
2215  |  FCGR3B  |  DISEASES
213  |  ALB  |  DISEASES
3600  |  IL15  |  DISEASES
7098  |  TLR3  |  DISEASES
55832  |  CAND1  |  DISEASES
4054  |  LTBP3  |  DISEASES
3233  |  HOXD4  |  DISEASES
83987  |  CCDC8  |  DISEASES
55699  |  IARS2  |  DISEASES
171558  |  PTCRA  |  DISEASES
10815  |  CPLX1  |  DISEASES
3627  |  CXCL10  |  DISEASES
50515  |  CHST11  |  DISEASES
3669  |  ISG20  |  DISEASES
6373  |  CXCL11  |  DISEASES
54205  |  CYCS  |  DISEASES
8487  |  GEMIN2  |  DISEASES
6363  |  CCL19  |  DISEASES
116028  |  RMI2  |  DISEASES
8636  |  SSNA1  |  DISEASES
203859  |  ANO5  |  DISEASES
1776  |  DNASE1L3  |  DISEASES
23129  |  PLXND1  |  DISEASES
8607  |  RUVBL1  |  DISEASES
4684  |  NCAM1  |  DISEASES
8834  |  TMEM11  |  DISEASES
80381  |  CD276  |  DISEASES
50628  |  GEMIN4  |  DISEASES
3039  |  HBA1  |  DISEASES
2200  |  FBN1  |  DISEASES
10250  |  SRRM1  |  DISEASES
51330  |  TNFRSF12A  |  DISEASES
3563  |  IL3RA  |  DISEASES
3665  |  IRF7  |  DISEASES
1915  |  EEF1A1  |  DISEASES
340061  |  TMEM173  |  DISEASES
8214  |  DGCR6  |  DISEASES
6401  |  SELE  |  DISEASES
942  |  CD86  |  DISEASES
3320  |  HSP90AA1  |  DISEASES
23336  |  SYNM  |  DISEASES
9138  |  ARHGEF1  |  DISEASES
123283  |  TARSL2  |  DISEASES
23583  |  SMUG1  |  DISEASES
3117  |  HLA-DQA1  |  DISEASES
7060  |  THBS4  |  DISEASES
3329  |  HSPD1  |  DISEASES
966  |  CD59  |  DISEASES
8805  |  TRIM24  |  DISEASES
2963  |  GTF2F2  |  DISEASES
1308  |  COL17A1  |  DISEASES
7137  |  TNNI3  |  DISEASES
6731  |  SRP72  |  DISEASES
3146  |  HMGB1  |  DISEASES
92399  |  MRRF  |  DISEASES
3605  |  IL17A  |  DISEASES
7332  |  UBE2L3  |  DISEASES
10617  |  STAMBP  |  DISEASES
9045  |  RPL14  |  DISEASES
10438  |  C1D  |  DISEASES
219844  |  HYLS1  |  DISEASES
1108  |  CHD4  |  DISEASES
6421  |  SFPQ  |  DISEASES
6597  |  SMARCA4  |  DISEASES
51592  |  TRIM33  |  DISEASES
6775  |  STAT4  |  DISEASES
405  |  ARNT  |  DISEASES
6364  |  CCL20  |  DISEASES
9332  |  CD163  |  DISEASES
26191  |  PTPN22  |  DISEASES
4151  |  MB  |  DISEASES
3123  |  HLA-DRB1  |  DISEASES
127343  |  DMBX1  |  DISEASES
170482  |  CLEC4C  |  DISEASES
23294  |  ANKS1A  |  DISEASES
54106  |  TLR9  |  DISEASES
56955  |  MEPE  |  DISEASES
6772  |  STAT1  |  DISEASES
7150  |  TOP1  |  DISEASES
4283  |  CXCL9  |  DISEASES
1756  |  DMD  |  DISEASES
3211  |  HOXB1  |  DISEASES
7052  |  TGM2  |  DISEASES
7042  |  TGFB2  |  DISEASES
6738  |  TROVE2  |  DISEASES
7402  |  UTRN  |  DISEASES
356  |  FASLG  |  DISEASES
2214  |  FCGR3A  |  DISEASES
51744  |  CD244  |  DISEASES
2205  |  FCER1A  |  DISEASES
911  |  CD1C  |  DISEASES
632  |  BGLAP  |  DISEASES
4580  |  MTX1  |  DISEASES
4582  |  MUC1  |  DISEASES
6280  |  S100A9  |  DISEASES
80222  |  TARS2  |  DISEASES
2018  |  EMX2  |  DISEASES
11218  |  DDX20  |  DISEASES
959  |  CD40LG  |  DISEASES
80351  |  TNKS2  |  DISEASES
1757  |  SARDH  |  DISEASES
6130  |  RPL7A  |  DISEASES
958  |  CD40  |  DISEASES
6441  |  SFTPD  |  DISEASES
1503  |  CTPS1  |  DISEASES
64102  |  TNMD  |  DISEASES
23452  |  ANGPTL2  |  DISEASES
8565  |  YARS  |  DISEASES
5928  |  RBBP4  |  DISEASES
2833  |  CXCR3  |  DISEASES
6118  |  RPA2  |  DISEASES
7099  |  TLR4  |  DISEASES
24137  |  KIF4A  |  DISEASES
3339  |  HSPG2  |  DISEASES
3108  |  HLA-DMA  |  DISEASES
5698  |  PSMB9  |  DISEASES
3118  |  HLA-DQA2  |  DISEASES
5081  |  PAX7  |  DISEASES
6499  |  SKIV2L  |  DISEASES
10673  |  TNFSF13B  |  DISEASES
50943  |  FOXP3  |  DISEASES
7133  |  TNFRSF1B  |  DISEASES
1041  |  CDSN  |  DISEASES
3105  |  HLA-A  |  DISEASES
5394  |  EXOSC10  |  DISEASES
7056  |  THBD  |  DISEASES
8718  |  TNFRSF25  |  DISEASES
57623  |  ZFAT  |  DISEASES
441376  |  AARD  |  DISEASES
51182  |  HSPA14  |  DISEASES
22929  |  SEPHS1  |  DISEASES
9308  |  CD83  |  DISEASES
9636  |  ISG15  |  DISEASES
5393  |  EXOSC9  |  DISEASES
1059  |  CENPB  |  DISEASES
23586  |  DDX58  |  DISEASES
3456  |  IFNB1  |  DISEASES
1107  |  CHD3  |  DISEASES
140462  |  ASB9  |  DISEASES
51284  |  TLR7  |  DISEASES
11168  |  PSIP1  |  DISEASES
11172  |  INSL6  |  DISEASES
131405  |  TRIM71  |  DISEASES
339965  |  CCDC158  |  DISEASES
4099  |  MAG  |  DISEASES
7341  |  SUMO1  |  DISEASES
2591  |  GALNT3  |  DISEASES
55601  |  DDX60  |  DISEASES
3885  |  KRT34  |  DISEASES
2962  |  GTF2F1  |  DISEASES
6696  |  SPP1  |  DISEASES
3965  |  LGALS9  |  DISEASES
6387  |  CXCL12  |  DISEASES
831  |  CAST  |  DISEASES
79168  |  LILRA6  |  DISEASES
825  |  CAPN3  |  DISEASES
4599  |  MX1  |  DISEASES
3119  |  HLA-DQB1  |  DISEASES
23515  |  MORC3  |  DISEASES
23308  |  ICOSLG  |  DISEASES
81493  |  SYNC  |  DISEASES
340351  |  AGBL3  |  DISEASES
3120  |  HLA-DQB2  |  DISEASES
6165  |  RPL35A  |  DISEASES
720  |  C4A  |  DISEASES
7124  |  TNF  |  DISEASES
5334  |  PLCL1  |  DISEASES
388372  |  CCL4L1  |  DISEASES
5378  |  PMS1  |  DISEASES
3115  |  HLA-DPB1  |  DISEASES
6358  |  CCL14  |  DISEASES
83871  |  RAB34  |  DISEASES
3586  |  IL10  |  DISEASES
10046  |  MAMLD1  |  DISEASES
721  |  C4B  |  DISEASES
389072  |  PLEKHM3  |  DISEASES
6168  |  RPL37A  |  DISEASES
51428  |  DDX41  |  DISEASES
3035  |  HARS  |  DISEASES
23741  |  EID1  |  DISEASES
22827  |  PUF60  |  DISEASES
930  |  CD19  |  DISEASES
3227  |  HOXC11  |  DISEASES
8742  |  TNFSF12  |  DISEASES
6625  |  SNRNP70  |  DISEASES
6029  |  RN7SL1  |  DISEASES
Locus(Waiting for update.)
Disease ID 66
Disease dermatomyositis
Integrated Phenotype
HPO | Name(Total Integrated Phenotypes:49)
HP:0011675  |  Arrhythmia
HP:0001618  |  Dysphonia
HP:0000492  |  Abnormality of the eyelid
HP:0002829  |  Arthralgia
HP:0001824  |  Weight loss
HP:0009071  |  Inflammatory myopathy
HP:0002092  |  Pulmonary arterial hypertension
HP:0100585  |  Telangiectasia of the skin
HP:0100723  |  Gastrointestinal stroma tumor
HP:0000934  |  Chondrocalcinosis
HP:0001879  |  Abnormality of eosinophils
HP:0000992  |  Cutaneous photosensitivity
HP:0003701  |  Proximal muscle weakness
HP:0002960  |  Autoimmunity
HP:0003326  |  Myalgia
HP:0001945  |  Fever
HP:0006530  |  Interstitial pulmonary disease
HP:0030078  |  Lung adenocarcinoma
HP:0002206  |  Pulmonary fibrosis
HP:0002207  |  Diffuse reticular or finely nodular infiltrations
HP:0000969  |  Edema
HP:0100758  |  Gangrene
HP:0002093  |  Respiratory insufficiency
HP:0200042  |  Skin ulcer
HP:0001252  |  Muscular hypotonia
HP:0003002  |  Breast carcinoma
HP:0002664  |  Neoplasm
HP:0011362  |  Abnormal hair quantity
HP:0003457  |  EMG abnormality
HP:0001063  |  Acrocyanosis
HP:0000989  |  Pruritus
HP:0001597  |  Abnormality of the nail
HP:0002633  |  Vasculitis
HP:0012378  |  Fatigue
HP:0001369  |  Arthritis
HP:0000958  |  Dry skin
HP:0001701  |  Pericarditis
HP:0100658  |  Cellulitis
HP:0008065  |  Aplasia/Hypoplasia of the skin
HP:0002205  |  Recurrent respiratory infections
HP:0002665  |  Lymphoma
HP:0012819  |  Myocarditis
HP:0100539  |  Periorbital edema
HP:0001658  |  Myocardial infarction
HP:0008872  |  Feeding difficulties in infancy
HP:0200034  |  Papule
HP:0001608  |  Abnormality of the voice
HP:0011703  |  Sinus tachycardia
HP:0010783  |  Erythema
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:73)
HP:0006530  |  Interstitial lung disease  |  25
HP:0002090  |  Pneumonia  |  10
HP:0003761  |  Calcinosis  |  8
HP:0002633  |  Vasculitis  |  5
HP:0030731  |  Carcinoma  |  5
HP:0001370  |  Rheumatoid arthritis  |  5
HP:0001369  |  Arthritis  |  5
HP:0000969  |  Dropsy  |  4
HP:0012490  |  Inflammation of fat tissue  |  3
HP:0003002  |  Breast carcinoma  |  3
HP:0002861  |  Melanoma  |  2
HP:0001324  |  Muscular weakness  |  2
HP:0100324  |  Progressive systemic scleroderma  |  2
HP:0002664  |  Neoplasia  |  2
HP:0002862  |  Bladder carcinoma  |  2
HP:0002094  |  Dyspnea  |  2
HP:0012115  |  Liver inflammation  |  2
HP:0200034  |  Papule  |  2
HP:0100614  |  Muscle inflammation  |  2
HP:0002725  |  Systemic lupus erythematosus  |  1
HP:0002583  |  Colitis  |  1
HP:0001907  |  Thromboembolic disease  |  1
HP:0000282  |  Facial puffiness  |  1
HP:0002273  |  Tetraparesis  |  1
HP:0001297  |  Cerebral vascular events  |  1
HP:0003323  |  Muscle weakness, progressive  |  1
HP:0002206  |  Pulmonary fibrosis  |  1
HP:0001649  |  Tachycardia  |  1
HP:0012226  |  Ovarian teratoma  |  1
HP:0009725  |  Bladder neoplasm  |  1
HP:0012378  |  Fatigue  |  1
HP:0011675  |  Arrhythmias  |  1
HP:0003201  |  Rhabdomyolysis  |  1
HP:0009125  |  Lipodystrophy  |  1
HP:0002829  |  Arthralgias  |  1
HP:0003701  |  Proximal limb muscle weakness  |  1
HP:0002875  |  Exertional dyspnea  |  1
HP:0002608  |  Celiac disease  |  1
HP:0001873  |  Low platelet count  |  1
HP:0002863  |  Myelodysplastic syndrome  |  1
HP:0003003  |  Colon cancer  |  1
HP:0002014  |  Diarrhea  |  1
HP:0011857  |  Plasmacytoma  |  1
HP:0002575  |  Tracheoesophageal fistula  |  1
HP:0002665  |  Lymphoma  |  1
HP:0030153  |  Cholangiocarcinoma  |  1
HP:0100646  |  Thyroiditis  |  1
HP:0004756  |  Ventricular tachycardia  |  1
HP:0100584  |  Endocarditis  |  1
HP:0100279  |  Ulcerative colitis  |  1
HP:0009792  |  Teratoma  |  1
HP:0000988  |  Exanthem  |  1
HP:0001061  |  Acne  |  1
HP:0003546  |  Exercise intolerance  |  1
HP:0030448  |  Soft tissue sarcoma  |  1
HP:0002592  |  Stomach ulcer  |  1
HP:0030357  |  Small cell lung carcinoma  |  1
HP:0002860  |  Squamous cell carcinoma  |  1
HP:0004808  |  Acute myelogenous leukemia  |  1
HP:0000099  |  Glomerular nephritis  |  1
HP:0000793  |  Membranoproliferative glomerulonephritis  |  1
HP:0001609  |  Hoarseness  |  1
HP:0003473  |  Fatigable weakness  |  1
HP:0000488  |  Noninflammatory retina disease  |  1
HP:0002960  |  Autoimmune condition  |  1
HP:0012126  |  Gastric cancer  |  1
HP:0010732  |  Nodular changes affecting the eyelids  |  1
HP:0002015  |  Swallowing difficulty  |  1
HP:0006689  |  Bacterial endocarditis  |  1
HP:0005681  |  Juvenile idiopathic arthritis  |  1
HP:0000872  |  Hashimoto's thyroiditis  |  1
HP:0010783  |  Erythema  |  1
HP:0000159  |  Lip abnormality  |  1
Disease ID 66
Disease dermatomyositis
Manually Symptom
UMLS  | Name(Total Manually Symptoms:153)
C2700478  |  meningioma
C2697424  |  gastric cancer
C2697391  |  rheumatoid arthritis
C2364133  |  infection
C2242539  |  subcutaneous infection
C1963274  |  vasculitis
C1963235  |  sick sinus syndrome
C1963220  |  pulmonary hypertension
C1963198  |  pancreatitis
C1963164  |  lymphopenia
C1963154  |  renal failure
C1963079  |  restrictive cardiomyopathy
C1962966  |  retinopathy
C1961102  |  acute lymphoblastic leukemia
C1959600  |  endomyocardial fibrosis
C1956346  |  coronary artery disease
C1704251  |  lymphoma of the breast
C1696156  |  pharyngeal necrosis
C1402315  |  vascular lesions
C1377913  |  pleural mesothelioma
C1333789  |  squamous cell carcinoma of the stomach
C1322286  |  thymic carcinoma
C1302772  |  cutaneous lymphoma
C1290344  |  nonspecific interstitial pneumonia
C1279945  |  acute interstitial pneumonia
C1262241  |  gastric melanoma
C1253937  |  pericardial effusion
C1145670  |  respiratory failure
C1140680  |  ovarian cancer
C1112565  |  pneumatosis intestinalis
C1096584  |  chlamydia pneumoniae infection
C1090821  |  sepsis
C1027109  |  scleroderma
C0947912  |  myasthenia
C0919642  |  ureteral necrosis
C0878544  |  myocardiopathies
C0751378  |  neurologic signs
C0748355  |  acute respiratory distress
C0748214  |  epidermoid carcinoma of the pyriform sinus
C0748159  |  pulmonary involvement
C0744422  |  diffuse proliferative glomerulonephritis
C0741949  |  cardiovascular pathology
C0740577  |  acute abdominal pain
C0699791  |  gastric carcinoma
C0678222  |  breast carcinoma
C0600139  |  carcinoma of the prostate
C0547058  |  pseudopolyposis
C0522224  |  palsy
C0520473  |  organic psychosis
C0473120  |  abdominal hematoma
C0410000  |  overlap syndrome
C0406650  |  linear iga bullous dermatosis
C0334663  |  true histiocytic lymphoma
C0334419  |  malignant pheochromocytoma
C0311343  |  membranous conjunctivitis
C0278584  |  metastatic carcinoma of the cervix
C0272126  |  evans' syndrome
C0267373  |  intestinal haemorrhage
C0267356  |  duodenal perforation
C0267063  |  cricopharyngeal achalasia
C0263627  |  calcinosis universalis
C0263367  |  koebner phenomenon
C0262988  |  cutaneous vasculitis
C0262941  |  myofasciitis
C0242770  |  bronchiolitis obliterans organizing pneumonia
C0242584  |  autoimmune thrombocytopenia
C0240035  |  interstitial pulmonary fibrosis
C0239946  |  liver fibrosis
C0238301  |  nasopharyngeal carcinoma
C0238301  |  nasopharyngeal cancer
C0238265  |  marchiafava-bignami disease
C0238115  |  spontaneous rupture of esophagus
C0221011  |  malignant atrophic papulosis
C0206698  |  cholangiocarcinoma
C0206695  |  neuroendocrine carcinoma
C0206178  |  cytomegalovirus retinitis
C0206178  |  cmv retinitis
C0206062  |  interstitial lung disease
C0206061  |  interstitial pneumonitis
C0206061  |  interstitial pneumonia
C0162855  |  mucinosis
C0162839  |  porokeratosis
C0155765  |  microangiopathy
C0155320  |  cortical blindness
C0153619  |  ureteral cancer
C0151436  |  cutaneous leukocytoclastic vasculitis
C0149871  |  deep venous thrombosis
C0085652  |  pyoderma gangrenosum
C0079772  |  t-cell lymphoma
C0079772  |  t cell lymphoma
C0079731  |  b-cell lymphoma
C0042769  |  virus infection
C0041834  |  erythema
C0041296  |  tuberculosis
C0040188  |  tic disorders
C0040034  |  thrombocytopenia
C0039103  |  synovitis
C0037285  |  skin manifestations
C0037285  |  skin manifestation
C0037284  |  skin lesions
C0037284  |  skin lesion
C0037274  |  skin disease
C0036262  |  scabies
C0036220  |  kaposi's sarcoma
C0035333  |  retinitis
C0034069  |  pulmonary fibrosis
C0034067  |  emphysema
C0033860  |  psoriasis
C0033771  |  prurigo
C0032266  |  pneumatosis cystoides intestinalis
C0030805  |  bullous pemphigoid
C0030781  |  peliosis hepatis
C0030436  |  parakeratosis
C0030326  |  panniculitis
C0029166  |  oral manifestations
C0029132  |  optic neuropathy
C0029089  |  ophthalmoplegia
C0027947  |  neutropenia
C0027051  |  myocardial infarction
C0026848  |  myopathy
C0026764  |  multiple myeloma
C0025517  |  metabolism disorders
C0024305  |  non-hodgkin's lymphoma
C0024299  |  lymphoma
C0024291  |  hemophagocytic syndrome
C0024291  |  haemophagocytic syndrome
C0023524  |  progressive multifocal leukoencephalopathy
C0022660  |  acute renal failure
C0021845  |  intestinal perforation
C0020758  |  ichthyosis
C0018799  |  heart disease
C0018799  |  diseases of the heart
C0017665  |  membranous nephropathy
C0017658  |  glomerulonephritis
C0015970  |  fever of unknown origin
C0015645  |  fasciitis
C0015230  |  skin rash
C0015230  |  skin eruption
C0015230  |  rashes
C0015230  |  rash
C0011168  |  dysphagia
C0009782  |  connective tissue disease
C0007286  |  carpal tunnel syndrome
C0007138  |  transitional cell carcinoma
C0006664  |  calcinosis cutis
C0006663  |  calcinosis
C0005742  |  blepharochalasis
C0003864  |  arthritides
C0002991  |  dermatofibromas
C0002880  |  autoimmune haemolytic anaemia
C0002726  |  amyloidosis
C0001815  |  idiopathic myelofibrosis
C0000889  |  acanthosis nigricans
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:33)
C0206062  |  interstitial lung disease  |  25
C0206061  |  interstitial pneumonia  |  13
C0006663  |  calcinosis  |  8
C0003873  |  rheumatoid arthritis  |  5
C0009450  |  infection  |  5
C0238301  |  nasopharyngeal carcinoma  |  4
C0042384  |  vasculitis  |  4
C0410000  |  overlap syndrome  |  4
C0030326  |  panniculitis  |  3
C0006664  |  calcinosis cutis  |  2
C1279945  |  acute interstitial pneumonia  |  2
C0015230  |  rash  |  2
C0011644  |  scleroderma  |  2
C0017658  |  glomerulonephritis  |  1
C0041834  |  erythema  |  1
C0034069  |  pulmonary fibrosis  |  1
C0042769  |  virus infection  |  1
C0263627  |  calcinosis universalis  |  1
C0024623  |  gastric cancer  |  1
C0947912  |  myasthenia  |  1
C0024299  |  lymphoma  |  1
C0206698  |  cholangiocarcinoma  |  1
C0040034  |  thrombocytopenia  |  1
C0155765  |  microangiopathy  |  1
C0009782  |  connective tissue disease  |  1
C0015230  |  skin rash  |  1
C0035309  |  retinopathy  |  1
C0011168  |  dysphagia  |  1
C0153392  |  nasopharyngeal cancer  |  1
C0744422  |  diffuse proliferative glomerulonephritis  |  1
C0037285  |  skin manifestations  |  1
C1140680  |  ovarian cancer  |  1
C0037284  |  skin lesion  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:12)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs10069690263205937015TERTumls:C0011633BeFreeChinese polymyositis (PM) patients (n =291), dermatomyositis (DM) patients (n=526) and ethnically-matched healthy controls (n =968) were genotyped for the CCL21 region SNPs (rs951005 and rs2492358), ERBB3 (rs2292239 and rs11171739), and TERT (rs2853676 and rs10069690), by using the Sequenom MassArray system.0.0002714422015TERT51279675CT
rs10069690263205936366CCL21umls:C0011633BeFreeChinese polymyositis (PM) patients (n =291), dermatomyositis (DM) patients (n=526) and ethnically-matched healthy controls (n =968) were genotyped for the CCL21 region SNPs (rs951005 and rs2492358), ERBB3 (rs2292239 and rs11171739), and TERT (rs2853676 and rs10069690), by using the Sequenom MassArray system.0.0029957922015TERT51279675CT
rs11171739263205937015TERTumls:C0011633BeFreeChinese polymyositis (PM) patients (n =291), dermatomyositis (DM) patients (n=526) and ethnically-matched healthy controls (n =968) were genotyped for the CCL21 region SNPs (rs951005 and rs2492358), ERBB3 (rs2292239 and rs11171739), and TERT (rs2853676 and rs10069690), by using the Sequenom MassArray system.0.0002714422015NA1256076841CT
rs11171739263205936366CCL21umls:C0011633BeFreeChinese polymyositis (PM) patients (n =291), dermatomyositis (DM) patients (n=526) and ethnically-matched healthy controls (n =968) were genotyped for the CCL21 region SNPs (rs951005 and rs2492358), ERBB3 (rs2292239 and rs11171739), and TERT (rs2853676 and rs10069690), by using the Sequenom MassArray system.0.0029957922015NA1256076841CT
rs2292239263205937015TERTumls:C0011633BeFreeChinese polymyositis (PM) patients (n =291), dermatomyositis (DM) patients (n=526) and ethnically-matched healthy controls (n =968) were genotyped for the CCL21 region SNPs (rs951005 and rs2492358), ERBB3 (rs2292239 and rs11171739), and TERT (rs2853676 and rs10069690), by using the Sequenom MassArray system.0.0002714422015ERBB31256088396TG
rs2292239263205936366CCL21umls:C0011633BeFreeChinese polymyositis (PM) patients (n =291), dermatomyositis (DM) patients (n=526) and ethnically-matched healthy controls (n =968) were genotyped for the CCL21 region SNPs (rs951005 and rs2492358), ERBB3 (rs2292239 and rs11171739), and TERT (rs2853676 and rs10069690), by using the Sequenom MassArray system.0.0029957922015ERBB31256088396TG
rs2492358263205937015TERTumls:C0011633BeFreeChinese polymyositis (PM) patients (n =291), dermatomyositis (DM) patients (n=526) and ethnically-matched healthy controls (n =968) were genotyped for the CCL21 region SNPs (rs951005 and rs2492358), ERBB3 (rs2292239 and rs11171739), and TERT (rs2853676 and rs10069690), by using the Sequenom MassArray system.0.0002714422015NA934737831CT
rs2492358263205936366CCL21umls:C0011633BeFreeChinese polymyositis (PM) patients (n =291), dermatomyositis (DM) patients (n=526) and ethnically-matched healthy controls (n =968) were genotyped for the CCL21 region SNPs (rs951005 and rs2492358), ERBB3 (rs2292239 and rs11171739), and TERT (rs2853676 and rs10069690), by using the Sequenom MassArray system.0.0029957922015NA934737831CT
rs2853676263205936366CCL21umls:C0011633BeFreeChinese polymyositis (PM) patients (n =291), dermatomyositis (DM) patients (n=526) and ethnically-matched healthy controls (n =968) were genotyped for the CCL21 region SNPs (rs951005 and rs2492358), ERBB3 (rs2292239 and rs11171739), and TERT (rs2853676 and rs10069690), by using the Sequenom MassArray system.0.0029957922015TERT51288432TC
rs2853676263205937015TERTumls:C0011633BeFreeChinese polymyositis (PM) patients (n =291), dermatomyositis (DM) patients (n=526) and ethnically-matched healthy controls (n =968) were genotyped for the CCL21 region SNPs (rs951005 and rs2492358), ERBB3 (rs2292239 and rs11171739), and TERT (rs2853676 and rs10069690), by using the Sequenom MassArray system.0.0002714422015TERT51288432TC
rs951005263205936366CCL21umls:C0011633BeFreeChinese polymyositis (PM) patients (n =291), dermatomyositis (DM) patients (n=526) and ethnically-matched healthy controls (n =968) were genotyped for the CCL21 region SNPs (rs951005 and rs2492358), ERBB3 (rs2292239 and rs11171739), and TERT (rs2853676 and rs10069690), by using the Sequenom MassArray system.0.0029957922015NA934743684GA
rs951005263205937015TERTumls:C0011633BeFreeChinese polymyositis (PM) patients (n =291), dermatomyositis (DM) patients (n=526) and ethnically-matched healthy controls (n =968) were genotyped for the CCL21 region SNPs (rs951005 and rs2492358), ERBB3 (rs2292239 and rs11171739), and TERT (rs2853676 and rs10069690), by using the Sequenom MassArray system.0.0002714422015NA934743684GA
GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)
GWASdb Snp Trait(Total Genotypes:6)
CHR POS SNPID REF ALT ORI_SNPID PMID P_VALUE P_VALUE_TEXT OR/BETA CI95_TEXT GWAS_INITIAL_SAMPLE_SIZE SUB_POPULATION SUPER_POPULATION GWAS_TRAIT HPO_ID HPO_TERM DO_ID DO_TERM MESH_ID MESH_TERM EFO_ID EFO_TERM DOLITE_TERM RISK_ALLELE PUBLICATION_TYPE AA GENE_SYMBOL TYPE REFGENE
2198780860rs938929AGrs938929239830888.32E-05NA1.22[1.10-1.34]1,178 European ancestry cases; 4,724 European ancestry controlsEuropean(5902)ALL(5902)EUR(5902)ALL(5902)DermatomyositisHPOID:0100614HPOID:0010978MyositisAbnormality of immune system physiologyDOID:10223dermatomyositisNANANANAPolymyositisNAResearch Support, Non-U.S. Gov't
2198809975rs1518364GArs1518364239830885.11E-05NA1.22[1.11-1.35]1,178 European ancestry cases; 4,724 European ancestry controlsEuropean(5902)ALL(5902)EUR(5902)ALL(5902)DermatomyositisHPOID:0100614HPOID:0010978MyositisAbnormality of immune system physiologyDOID:10223dermatomyositisNANANANAPolymyositisNAResearch Support, Non-U.S. Gov't
2198929806rs7572733CTrs7572733239830886.00E-06NA1.25[1.14-1.39]1,178 European ancestry cases; 4,724 European ancestry controlsEuropean(5902)ALL(5902)EUR(5902)ALL(5902)DermatomyositisHPOID:0100614HPOID:0010978MyositisAbnormality of immune system physiologyDOID:10223dermatomyositisNANANANAPolymyositisNAResearch Support, Non-U.S. Gov't
811343973rs2736340CTrs2736340239830886.53E-05NA1.25[1.12-1.40]1,178 European ancestry cases; 4,724 European ancestry controlsEuropean(5902)ALL(5902)EUR(5902)ALL(5902)DermatomyositisHPOID:0100614HPOID:0010978MyositisAbnormality of immune system physiologyDOID:10223dermatomyositisNANANANAPolymyositisNAResearch Support, Non-U.S. Gov't
934737828rs2492358CTrs2492358239830882.09E-04NA1.3[1.14-1.49]1,178 European ancestry cases; 4,724 European ancestry controlsEuropean(5902)ALL(5902)EUR(5902)ALL(5902)DermatomyositisHPOID:0100614HPOID:0010978MyositisAbnormality of immune system physiologyDOID:10223dermatomyositisNANANANAPolymyositisNAResearch Support, Non-U.S. Gov't
934743681rs951005GArs951005239830883.17E-04NA1.3[1.12-1.49]1,178 European ancestry cases; 4,724 European ancestry controlsEuropean(5902)ALL(5902)EUR(5902)ALL(5902)DermatomyositisHPOID:0100614HPOID:0010978MyositisAbnormality of immune system physiologyDOID:10223dermatomyositisNANANANAPolymyositisNAResearch Support, Non-U.S. Gov't
Mapped by lexical matching(Total Items:0)
(Waiting for update.)
Mapped by homologous gene(Total Items:0)
(Waiting for update.)
Chemical(Total Drugs:9)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0011633cyclophosphamideD00352050-18-0dermatomyositisMESH:D003882marker/mechanism12492978
C0011633diclofenacD00400815307-86-5dermatomyositisMESH:D003882marker/mechanism2917682
C0011633fluorouracilD00547251-21-8dermatomyositisMESH:D003882marker/mechanism18424388
C0011633hydroxyureaD006918127-07-1dermatomyositisMESH:D003882marker/mechanism18625537
C0011633lovastatinD00814875330-75-5dermatomyositisMESH:D003882marker/mechanism8944218
C0011633methotrexateD0087271959/5/2dermatomyositisMESH:D003882therapeutic20191521
C0011633omeprazoleD00985373590-58-6dermatomyositisMESH:D003882marker/mechanism16445794
C0011633phenytoinD01067257-41-0dermatomyositisMESH:D003882marker/mechanism9853654
C0011633pravastatinD01703581093-37-0dermatomyositisMESH:D003882marker/mechanism16154665
FDA approved drug and dosage information(Total Drugs:5)
DiseaseID Drug_name active_ingredients strength Dosage Form/Route Marketing Status TE code RLD RS
MESH:D003882mevacorlovastatin10MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasonsTABLET;ORALDiscontinuedNoneYesNo
MESH:D003882prilosecomeprazole20MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasonsCAPSULE, DELAYED REL PELLETS;ORALDiscontinuedNoneYesNo
MESH:D003882prilosecomeprazole20MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasonsCAPSULE, DELAYED REL PELLETS;ORALDiscontinuedNoneYesNo
MESH:D003882omeprazoleomeprazole20MGTABLET, DELAYED RELEASE;ORALOver-the-counterNoneYesYes
MESH:D003882omeprazoleomeprazole20MGTABLET, DELAYED RELEASE;ORALOver-the-counterNoneYesYes
FDA labeling changes(Total Drugs:5)
DiseaseID Pediatric_Labeling_Date Trade_Name Generic_Name_or_Proper_Name Indications Studied Label Changes Summary Product Labeling BPCA(B) PREA(P) BPCA(B) and PREA(P) Pediatric Rule (R) Sponsor Pediatric Exclusivity Granted Date NNPS
MESH:D00388202/14/2002mevacorlovastatinHeterozygous Familial HypercholesterolemiaNew indication in adolescent boys and girls (at least one year post-menarche) 10-17 years of ageLabelingB---Merck07/17/2001FALSE'
MESH:D00388212/7/2002prilosecomeprazoleGastroesophageal reflux and erosive esophagitisSafety and effectiveness established in pediatric patients 2-16 years of age Information on dose, PK parameters, exposure/response and AE profileLabelingB---AstraZeneca-FALSE'
MESH:D00388203/20/2008prilosecomeprazoleMaintenance healing of erosive esophagitisEfficacy was extrapolated from adults and older children to 1 to 2 year olds and supported with an open-label trial Unique adverse reactions in pediatric patients included increased respiratory system adverse events and fever. Safety and effectiveness in children less than 1 year of age have not been established Dosing and administration information provided for patients 1 year and older weighing at least 5 kg. New dosage formLabeling--B, P-AstraZeneca1/5/2001FALSE'
MESH:D00388212/7/2002prilosecomeprazoleGastroesophageal reflux and erosive esophagitisSafety and effectiveness established in pediatric patients 2-16 years of age Information on dose, PK parameters, exposure/response and AE profileLabelingB---AstraZeneca-FALSE'
MESH:D00388203/20/2008prilosecomeprazoleMaintenance healing of erosive esophagitisEfficacy was extrapolated from adults and older children to 1 to 2 year olds and supported with an open-label trial Unique adverse reactions in pediatric patients included increased respiratory system adverse events and fever. Safety and effectiveness in children less than 1 year of age have not been established Dosing and administration information provided for patients 1 year and older weighing at least 5 kg. New dosage formLabeling--B, P-AstraZeneca1/5/2001FALSE'