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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine



   myositis
  

Disease ID 493
Disease myositis
Definition
Inflammation of a muscle or muscle tissue.
Synonym
inflamm muscle dis
inflamm myopathy
inflammation of the skeletal muscle
inflammatory disorder of muscle
inflammatory disorder of muscle (disorder)
inflammatory muscle disease
inflammatory muscle diseases
inflammatory myopathies
inflammatory myopathy
inflammatory myopathy nos
muscle dis inflamm
muscle disease, inflammatory
muscle diseases, inflammatory
muscle inflammation
myopathies, inflammatory
myopathy inflamm
myopathy, inflammatory
myositides
myositis (disorder)
myositis [disease/finding]
myositis nos
myositis unspecified
myositis unspecified (disorder)
myositis, nos
OMIM
DOID
UMLS
C0027121
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:129)
C0024115  |  lung disease  |  13
C0206062  |  interstitial lung disease  |  12
C0026848  |  myopathy  |  5
C0011633  |  dermatomyositis  |  5
C0026850  |  muscular dystrophy  |  5
C0027121  |  myositis  |  4
C0021400  |  influenza  |  4
C0029401  |  paget's disease  |  4
C0003873  |  rheumatoid arthritis  |  4
C0003864  |  arthritis  |  4
C0409974  |  lupus erythematosus  |  4
C0027121  |  inflammatory myopathy  |  3
C0085655  |  polymyositis  |  3
C1527336  |  sjogren's syndrome  |  3
C0036421  |  systemic sclerosis  |  3
C0024141  |  systemic lupus erythematosus  |  3
C0009782  |  connective tissue disease  |  3
C0029089  |  ophthalmoplegia  |  3
C0032285  |  pneumonia  |  2
C0042769  |  viral infection  |  2
C0022660  |  acute renal failure  |  2
C0009319  |  colitis  |  2
C0040896  |  trichinellosis  |  2
C0011603  |  dermatitis  |  2
C0027059  |  myocarditis  |  2
C0011644  |  scleroderma  |  2
C0015645  |  fasciitis  |  2
C0023418  |  leukemia  |  2
C0010346  |  crohn's disease  |  2
C0015230  |  rash  |  2
C0029401  |  paget's disease of the bone  |  2
C0023470  |  myelocytic leukemia  |  1
C0162674  |  progressive external ophthalmoplegia  |  1
C0043117  |  idiopathic thrombocytopenic purpura  |  1
C0541912  |  duodenal ca  |  1
C0042164  |  intraocular inflammation  |  1
C0020437  |  hypercalcemia  |  1
C0017662  |  membranoproliferative glomerulonephritis  |  1
C0035934  |  rubinstein-taybi syndrome  |  1
C0085273  |  parvovirus b19 infection  |  1
C0026846  |  muscle atrophy  |  1
C0018378  |  guillain-barre syndrome  |  1
C0023487  |  acute promyelocytic leukemia  |  1
C0152013  |  lung adenocarcinoma  |  1
C0162674  |  chronic progressive external ophthalmoplegia  |  1
C0031069  |  familial mediterranean fever  |  1
C0270952  |  oculopharyngeal muscular dystrophy  |  1
C0036202  |  sarcoidosis  |  1
C0018213  |  graves' disease  |  1
C0036420  |  localized scleroderma  |  1
C0238190  |  inclusion body myositis  |  1
C0035078  |  renal failure  |  1
C0042769  |  viral infections  |  1
C0042373  |  vascular disorder  |  1
C0027121  |  muscle inflammation  |  1
C0026848  |  myopathies  |  1
C0242770  |  cryptogenic organizing pneumonia  |  1
C0032285  |  pneumoniae  |  1
C0029463  |  osteosarcoma  |  1
C0028754  |  adiposity  |  1
C0042373  |  vascular disorders  |  1
C0476089  |  endometrial carcinoma  |  1
C0235618  |  proliferative glomerulonephritis  |  1
C0027765  |  nervous system disease  |  1
C0432528  |  proliferative fasciitis  |  1
C0206642  |  parosteal osteosarcoma  |  1
C0398794  |  griscelli syndrome  |  1
C0001418  |  adenocarcinoma  |  1
C0024198  |  lyme disease  |  1
C0017160  |  gastroenteritis  |  1
C0004943  |  behcet's disease  |  1
C0036421  |  systemic scleroderma  |  1
C0021053  |  immune disease  |  1
C0032285  |  lung inflammation  |  1
C0023473  |  chronic myelogenous leukemia  |  1
C0007194  |  hypertrophic cardiomyopathy  |  1
C0029132  |  optic neuropathy  |  1
C1704275  |  pyomyositis  |  1
C0028064  |  niemann-pick disease  |  1
C0026848  |  muscle disease  |  1
C0007138  |  urothelial carcinoma  |  1
C0007102  |  colon cancer  |  1
C0023473  |  chronic myeloid leukemia  |  1
C0278846  |  invasive thymoma  |  1
C0017105  |  gas gangrene  |  1
C0023487  |  promyelocytic leukemia  |  1
C0034735  |  raynaud phenomenon  |  1
C0023470  |  myeloid leukemia  |  1
C0007570  |  celiac disease  |  1
C0235974  |  pancreatic cancer  |  1
C0019291  |  hiatus hernia  |  1
C0032541  |  polyneuritis  |  1
C0022116  |  ischemia  |  1
C0023492  |  t-cell leukemia  |  1
C0040188  |  tic disorders  |  1
C0009782  |  connective tissue diseases  |  1
C0236642  |  pick disease  |  1
C0009324  |  ulcerative colitis  |  1
C0022661  |  chronic renal failure  |  1
C0010068  |  coronary artery disease  |  1
C0040100  |  thymoma  |  1
C0034735  |  raynaud's phenomenon  |  1
C1370740  |  adrenal carcinoma  |  1
C0007682  |  central nervous system disease  |  1
C0206141  |  hypereosinophilic syndrome  |  1
C0007134  |  renal carcinoma  |  1
C0476089  |  endometrial ca  |  1
C0085273  |  erythema infectiosum  |  1
C0024302  |  large cell lymphoma  |  1
C0021053  |  immune disorder  |  1
C0042721  |  viral hepatitis  |  1
C0021845  |  bowel perforation  |  1
C0024143  |  lupus nephritis  |  1
C0018802  |  congestive cardiac failure  |  1
C0002395  |  alzheimer's disease  |  1
C0206180  |  anaplastic large cell lymphoma  |  1
C1258104  |  diffuse systemic sclerosis  |  1
C0021831  |  bowel disease  |  1
C0023895  |  liver disease  |  1
C0008728  |  churg-strauss syndrome  |  1
C0027697  |  nephritis  |  1
C0021390  |  inflammatory bowel disease  |  1
C0035412  |  rhabdomyosarcoma  |  1
C0026272  |  mixed connective tissue disease  |  1
C0456909  |  vision loss  |  1
C0018801  |  cardiac failure  |  1
C0023470  |  myelogenous leukemia  |  1
C0042384  |  angiitis  |  1
C0042870  |  vitamin d defic  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:6)
3514  |  IGKC  |  CTD_human
6897  |  TARS  |  CTD_human
3557  |  IL1RN  |  CTD_human
10020  |  GNE  |  GHR
3500  |  IGHG1  |  CTD_human
3501  |  IGHG2  |  CTD_human
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:11)
3117  |  HLA-DQA1  |  CIPHER
3119  |  HLA-DQB1  |  CIPHER
3123  |  HLA-DRB1  |  CIPHER
2214  |  FCGR3A  |  CIPHER
3106  |  HLA-B  |  CIPHER
26191  |  PTPN22  |  CIPHER
3514  |  IGKC  |  CTD_human
6897  |  TARS  |  CTD_human
3501  |  IGHG2  |  CTD_human
3557  |  IL1RN  |  CTD_human
3500  |  IGHG1  |  CTD_human
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:264)
441376  |  AARD  |  1.728  |  DISEASES
60  |  ACTB  |  1.597  |  DISEASES
10555  |  AGPAT2  |  1.36  |  DISEASES
64400  |  AKTIP  |  2.479  |  DISEASES
238  |  ALK  |  1.681  |  DISEASES
270  |  AMPD1  |  1.239  |  DISEASES
272  |  AMPD3  |  1.135  |  DISEASES
23452  |  ANGPTL2  |  1.261  |  DISEASES
140462  |  ASB9  |  1.771  |  DISEASES
9474  |  ATG5  |  1.308  |  DISEASES
538  |  ATP7A  |  2.21  |  DISEASES
11273  |  ATXN2L  |  1.275  |  DISEASES
567  |  B2M  |  1.375  |  DISEASES
100379571  |  BACE1-AS  |  1.5  |  DISEASES
25825  |  BACE2  |  1.623  |  DISEASES
627  |  BDNF  |  2.005  |  DISEASES
8678  |  BECN1  |  1.076  |  DISEASES
632  |  BGLAP  |  1.574  |  DISEASES
388552  |  BLOC1S3  |  1.319  |  DISEASES
26580  |  BSCL2  |  1.156  |  DISEASES
56244  |  BTNL2  |  1.48  |  DISEASES
10438  |  C1D  |  1.45  |  DISEASES
149466  |  C1orf210  |  1.433  |  DISEASES
720  |  C4A  |  2.241  |  DISEASES
721  |  C4B  |  1.368  |  DISEASES
796  |  CALCA  |  1.206  |  DISEASES
820  |  CAMP  |  2.195  |  DISEASES
825  |  CAPN3  |  3.216  |  DISEASES
834  |  CASP1  |  1.033  |  DISEASES
339965  |  CCDC158  |  1.911  |  DISEASES
388372  |  CCL4L1  |  1.508  |  DISEASES
6354  |  CCL7  |  1.53  |  DISEASES
6355  |  CCL8  |  2.519  |  DISEASES
1232  |  CCR3  |  1.889  |  DISEASES
9332  |  CD163  |  2.681  |  DISEASES
930  |  CD19  |  2.078  |  DISEASES
911  |  CD1C  |  1.151  |  DISEASES
914  |  CD2  |  2.52  |  DISEASES
51744  |  CD244  |  1.363  |  DISEASES
958  |  CD40  |  1.146  |  DISEASES
959  |  CD40LG  |  4.24  |  DISEASES
921  |  CD5  |  2.264  |  DISEASES
966  |  CD59  |  1.07  |  DISEASES
942  |  CD86  |  1.163  |  DISEASES
1041  |  CDSN  |  4.183  |  DISEASES
1059  |  CENPB  |  2.281  |  DISEASES
1108  |  CHD4  |  2.398  |  DISEASES
63924  |  CIDEC  |  1.759  |  DISEASES
548596  |  CKMT1A  |  1.695  |  DISEASES
170482  |  CLEC4C  |  2.843  |  DISEASES
7555  |  CNBP  |  1.924  |  DISEASES
1268  |  CNR1  |  1.365  |  DISEASES
22796  |  COG2  |  1.075  |  DISEASES
255631  |  COL24A1  |  1.977  |  DISEASES
1312  |  COMT  |  3.119  |  DISEASES
1520  |  CTSS  |  1.325  |  DISEASES
4283  |  CXCL9  |  2.768  |  DISEASES
2833  |  CXCR3  |  2.779  |  DISEASES
50626  |  CYHR1  |  1.568  |  DISEASES
1565  |  CYP2D6  |  1.204  |  DISEASES
51428  |  DDX41  |  2.572  |  DISEASES
9879  |  DDX46  |  1.718  |  DISEASES
23586  |  DDX58  |  1.739  |  DISEASES
55601  |  DDX60  |  1.602  |  DISEASES
8214  |  DGCR6  |  1.291  |  DISEASES
127343  |  DMBX1  |  2.274  |  DISEASES
1756  |  DMD  |  3.222  |  DISEASES
8291  |  DYSF  |  2.981  |  DISEASES
1915  |  EEF1A1  |  1.357  |  DISEASES
23741  |  EID1  |  1.479  |  DISEASES
2010  |  EMD  |  1.924  |  DISEASES
2036  |  EPB41L1  |  1.09  |  DISEASES
2042  |  EPHA3  |  1.003  |  DISEASES
30816  |  ERVW-1  |  1.006  |  DISEASES
5394  |  EXOSC10  |  5.822  |  DISEASES
5393  |  EXOSC9  |  3.998  |  DISEASES
355  |  FAS  |  1.507  |  DISEASES
114907  |  FBXO32  |  1.408  |  DISEASES
26190  |  FBXW2  |  1.708  |  DISEASES
2205  |  FCER1A  |  1.022  |  DISEASES
2214  |  FCGR3A  |  1.552  |  DISEASES
79147  |  FKRP  |  2.584  |  DISEASES
2332  |  FMR1  |  1.587  |  DISEASES
221937  |  FOXK1  |  1.159  |  DISEASES
50943  |  FOXP3  |  1.704  |  DISEASES
2591  |  GALNT3  |  3.287  |  DISEASES
2624  |  GATA2  |  1.588  |  DISEASES
152007  |  GLIPR2  |  1.618  |  DISEASES
10020  |  GNE  |  6.704  |  DISEASES
2879  |  GPX4  |  2.48  |  DISEASES
2934  |  GSN  |  1.137  |  DISEASES
2961  |  GTF2E2  |  2.113  |  DISEASES
2962  |  GTF2F1  |  1.868  |  DISEASES
2963  |  GTF2F2  |  1.774  |  DISEASES
3035  |  HARS  |  5.165  |  DISEASES
3105  |  HLA-A  |  1.694  |  DISEASES
3108  |  HLA-DMA  |  2.343  |  DISEASES
3115  |  HLA-DPB1  |  2.102  |  DISEASES
3117  |  HLA-DQA1  |  3.384  |  DISEASES
3118  |  HLA-DQA2  |  1.662  |  DISEASES
3119  |  HLA-DQB1  |  1.789  |  DISEASES
3120  |  HLA-DQB2  |  1.417  |  DISEASES
3123  |  HLA-DRB1  |  3.373  |  DISEASES
3146  |  HMGB1  |  1.641  |  DISEASES
3181  |  HNRNPA2B1  |  1.304  |  DISEASES
3227  |  HOXC11  |  1.131  |  DISEASES
3320  |  HSP90AA1  |  1.398  |  DISEASES
51182  |  HSPA14  |  1.026  |  DISEASES
3304  |  HSPA1B  |  1.52  |  DISEASES
3329  |  HSPD1  |  1.308  |  DISEASES
3339  |  HSPG2  |  3.651  |  DISEASES
3356  |  HTR2A  |  2.446  |  DISEASES
3359  |  HTR3A  |  3.46  |  DISEASES
3363  |  HTR7  |  2.367  |  DISEASES
23308  |  ICOSLG  |  2.953  |  DISEASES
3620  |  IDO1  |  1.426  |  DISEASES
3434  |  IFIT1  |  1.09  |  DISEASES
3437  |  IFIT3  |  1.368  |  DISEASES
3456  |  IFNB1  |  2.871  |  DISEASES
3586  |  IL10  |  2.775  |  DISEASES
3605  |  IL17A  |  2.789  |  DISEASES
3559  |  IL2RA  |  1.362  |  DISEASES
3563  |  IL3RA  |  2.792  |  DISEASES
11172  |  INSL6  |  1.735  |  DISEASES
3665  |  IRF7  |  1.119  |  DISEASES
9636  |  ISG15  |  2.235  |  DISEASES
3684  |  ITGAM  |  1.479  |  DISEASES
50618  |  ITSN2  |  2.273  |  DISEASES
102723508  |  KANTR  |  2.492  |  DISEASES
3739  |  KCNA4  |  2.404  |  DISEASES
24137  |  KIF4A  |  1.064  |  DISEASES
3885  |  KRT34  |  1.682  |  DISEASES
3908  |  LAMA2  |  1.405  |  DISEASES
3920  |  LAMP2  |  1.353  |  DISEASES
11155  |  LDB3  |  2.177  |  DISEASES
79168  |  LILRA6  |  1.504  |  DISEASES
4094  |  MAF  |  1.15  |  DISEASES
4137  |  MAPT  |  1.693  |  DISEASES
4151  |  MB  |  3.956  |  DISEASES
79104  |  MEG8  |  1.582  |  DISEASES
8972  |  MGAM  |  1.95  |  DISEASES
4311  |  MME  |  1.342  |  DISEASES
23515  |  MORC3  |  5.686  |  DISEASES
84545  |  MRPL43  |  2.129  |  DISEASES
4553  |  MT-TA  |  1.055  |  DISEASES
4582  |  MUC1  |  3.583  |  DISEASES
4599  |  MX1  |  3.145  |  DISEASES
4615  |  MYD88  |  1.126  |  DISEASES
4624  |  MYH6  |  2.059  |  DISEASES
4625  |  MYH7  |  1.744  |  DISEASES
79903  |  NAA60  |  1.74  |  DISEASES
4077  |  NBR1  |  1.794  |  DISEASES
4712  |  NDUFB6  |  1.452  |  DISEASES
4703  |  NEB  |  1.122  |  DISEASES
4803  |  NGF  |  1.69  |  DISEASES
114548  |  NLRP3  |  1.046  |  DISEASES
594857  |  NPS  |  3.188  |  DISEASES
4988  |  OPRM1  |  2.057  |  DISEASES
5025  |  P2RX4  |  1.148  |  DISEASES
5081  |  PAX7  |  2.139  |  DISEASES
9260  |  PDLIM7  |  1.333  |  DISEASES
11331  |  PHB2  |  1.776  |  DISEASES
5334  |  PLCL1  |  2.555  |  DISEASES
389072  |  PLEKHM3  |  2.662  |  DISEASES
5378  |  PMS1  |  1.762  |  DISEASES
5406  |  PNLIP  |  1.845  |  DISEASES
5535  |  PPP3R2  |  1.78  |  DISEASES
5550  |  PREP  |  1.787  |  DISEASES
5621  |  PRNP  |  1.212  |  DISEASES
5627  |  PROS1  |  2.041  |  DISEASES
11168  |  PSIP1  |  2.522  |  DISEASES
5699  |  PSMB10  |  1.38  |  DISEASES
5696  |  PSMB8  |  2.834  |  DISEASES
5698  |  PSMB9  |  1.862  |  DISEASES
26191  |  PTPN22  |  1.251  |  DISEASES
5788  |  PTPRC  |  1.496  |  DISEASES
284119  |  PTRF  |  1.168  |  DISEASES
22827  |  PUF60  |  1.911  |  DISEASES
5928  |  RBBP4  |  1.337  |  DISEASES
6029  |  RN7SL1  |  1.306  |  DISEASES
6048  |  RNF5  |  1.433  |  DISEASES
9045  |  RPL14  |  1.224  |  DISEASES
6168  |  RPL37A  |  1.257  |  DISEASES
6130  |  RPL7A  |  1.212  |  DISEASES
57142  |  RTN4  |  1.5  |  DISEASES
6280  |  S100A9  |  1.959  |  DISEASES
6295  |  SAG  |  1.091  |  DISEASES
1757  |  SARDH  |  2.934  |  DISEASES
54938  |  SARS2  |  1.112  |  DISEASES
6335  |  SCN9A  |  2.002  |  DISEASES
6401  |  SELE  |  1.687  |  DISEASES
22929  |  SEPHS1  |  1.427  |  DISEASES
5265  |  SERPINA1  |  3.869  |  DISEASES
12  |  SERPINA3  |  1.95  |  DISEASES
6441  |  SFTPD  |  2.433  |  DISEASES
6533  |  SLC6A6  |  1.302  |  DISEASES
6597  |  SMARCA4  |  1.77  |  DISEASES
27293  |  SMPDL3B  |  1.522  |  DISEASES
55234  |  SMU1  |  1.462  |  DISEASES
23583  |  SMUG1  |  2.771  |  DISEASES
619498  |  SNORD74  |  1.927  |  DISEASES
6625  |  SNRNP70  |  4.989  |  DISEASES
6635  |  SNRPE  |  1.2  |  DISEASES
79582  |  SPAG16  |  1.081  |  DISEASES
10615  |  SPAG5  |  1.043  |  DISEASES
6693  |  SPN  |  1.678  |  DISEASES
6696  |  SPP1  |  1.122  |  DISEASES
8878  |  SQSTM1  |  2.717  |  DISEASES
6731  |  SRP72  |  1.792  |  DISEASES
10250  |  SRRM1  |  1.521  |  DISEASES
10617  |  STAMBP  |  1.113  |  DISEASES
6772  |  STAT1  |  1.659  |  DISEASES
6775  |  STAT4  |  1.812  |  DISEASES
8677  |  STX10  |  2.347  |  DISEASES
8801  |  SUCLG2  |  1.496  |  DISEASES
7341  |  SUMO1  |  1.042  |  DISEASES
81493  |  SYNC  |  1.101  |  DISEASES
23336  |  SYNM  |  1.94  |  DISEASES
284612  |  SYPL2  |  1.717  |  DISEASES
6863  |  TAC1  |  4.165  |  DISEASES
80222  |  TARS2  |  4.47  |  DISEASES
123283  |  TARSL2  |  4.506  |  DISEASES
6999  |  TDO2  |  1.03  |  DISEASES
7052  |  TGM2  |  1.552  |  DISEASES
7056  |  THBD  |  1.247  |  DISEASES
7060  |  THBS4  |  1.531  |  DISEASES
7072  |  TIA1  |  3.852  |  DISEASES
7099  |  TLR4  |  1.818  |  DISEASES
51284  |  TLR7  |  1.39  |  DISEASES
54106  |  TLR9  |  1.351  |  DISEASES
7124  |  TNF  |  4.213  |  DISEASES
8792  |  TNFRSF11A  |  1.162  |  DISEASES
51330  |  TNFRSF12A  |  1.338  |  DISEASES
7133  |  TNFRSF1B  |  3.699  |  DISEASES
8718  |  TNFRSF25  |  3.729  |  DISEASES
8742  |  TNFSF12  |  1.131  |  DISEASES
10673  |  TNFSF13B  |  2.819  |  DISEASES
64102  |  TNMD  |  1.822  |  DISEASES
7137  |  TNNI3  |  1.742  |  DISEASES
7139  |  TNNT2  |  1.716  |  DISEASES
10953  |  TOMM34  |  1.108  |  DISEASES
7150  |  TOP1  |  2.695  |  DISEASES
1861  |  TOR1A  |  1.355  |  DISEASES
7169  |  TPM2  |  1.227  |  DISEASES
8805  |  TRIM24  |  3.582  |  DISEASES
7706  |  TRIM25  |  1.205  |  DISEASES
51592  |  TRIM33  |  5.042  |  DISEASES
131405  |  TRIM71  |  1.33  |  DISEASES
6738  |  TROVE2  |  4.123  |  DISEASES
7442  |  TRPV1  |  1.62  |  DISEASES
51393  |  TRPV2  |  1.023  |  DISEASES
7273  |  TTN  |  3.085  |  DISEASES
7311  |  UBA52  |  1.29  |  DISEASES
7332  |  UBE2L3  |  1.409  |  DISEASES
9354  |  UBE4A  |  2.295  |  DISEASES
10277  |  UBE4B  |  1.76  |  DISEASES
7402  |  UTRN  |  1.942  |  DISEASES
7415  |  VCP  |  4.138  |  DISEASES
7422  |  VEGFA  |  1.25  |  DISEASES
57623  |  ZFAT  |  1.262  |  DISEASES
10269  |  ZMPSTE24  |  1.091  |  DISEASES
6940  |  ZNF354A  |  1.442  |  DISEASES
117608  |  ZNF354B  |  2.081  |  DISEASES
30832  |  ZNF354C  |  1.626  |  DISEASES
Locus(Waiting for update.)
Disease ID 493
Disease myositis
Integrated Phenotype
HPO | Name(Total Integrated Phenotypes:2)
HP:0003701  |  Proximal limb muscle weakness
HP:0100614  |  Muscle inflammation
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:92)
HP:0006530  |  Interstitial lung disease  |  12
HP:0001324  |  Muscular weakness  |  10
HP:0003201  |  Rhabdomyolysis  |  8
HP:0003198  |  Myopathic changes  |  5
HP:0100614  |  Muscle inflammation  |  5
HP:0003560  |  Muscular dystrophy  |  5
HP:0001369  |  Arthritis  |  4
HP:0001370  |  Rheumatoid arthritis  |  4
HP:0012531  |  Pain  |  4
HP:0000602  |  Ophthalmoplegia  |  4
HP:0000969  |  Dropsy  |  4
HP:0002015  |  Swallowing difficulty  |  4
HP:0003326  |  Muscle pain  |  3
HP:0002725  |  Systemic lupus erythematosus  |  3
HP:0009071  |  Inflammatory myopathy  |  3
HP:0003701  |  Proximal limb muscle weakness  |  3
HP:0003236  |  Elevated creatine kinase  |  3
HP:0002583  |  Colitis  |  2
HP:0100537  |  Inflammation of the fascia  |  2
HP:0100324  |  Progressive systemic scleroderma  |  2
HP:0001909  |  Leukemia  |  2
HP:0030731  |  Carcinoma  |  2
HP:0003805  |  Rimmed vacuoles  |  2
HP:0001945  |  Fever  |  2
HP:0002090  |  Pneumonia  |  2
HP:0002910  |  Elevated transaminases  |  2
HP:0001919  |  Acute renal failure  |  2
HP:0000988  |  Exanthem  |  2
HP:0000544  |  CPEO  |  2
HP:0030880  |  Raynaud phenomenon  |  2
HP:0001880  |  Eosinophilia  |  2
HP:0100280  |  Morbus Crohn  |  2
HP:0012819  |  Myocarditis  |  2
HP:0007417  |  Discoid lupus erythematosus  |  2
HP:0002633  |  Vasculitis  |  1
HP:0002527  |  Falls  |  1
HP:0002859  |  Rhabdomyosarcoma  |  1
HP:0003003  |  Colon cancer  |  1
HP:0000083  |  Renal insufficiency  |  1
HP:0200034  |  Papule  |  1
HP:0001288  |  Gait disturbance  |  1
HP:0001289  |  Confusion  |  1
HP:0010783  |  Erythema  |  1
HP:0045029  |  Eosinophilic fasciitis  |  1
HP:0000155  |  Oral ulcer  |  1
HP:0003323  |  Muscle weakness, progressive  |  1
HP:0100522  |  Thymoma  |  1
HP:0012473  |  Wasting of the tongue  |  1
HP:0012324  |  Myeloid leukemia  |  1
HP:0000590  |  Progressive external ophthalmoplegia  |  1
HP:0001349  |  Facial paresis, bilateral  |  1
HP:0001677  |  Coronary artery disease  |  1
HP:0002669  |  Osteosarcoma  |  1
HP:0002664  |  Neoplasia  |  1
HP:0000572  |  Visual loss  |  1
HP:0030664  |  Beevor's sign  |  1
HP:0001635  |  Congestive heart failure  |  1
HP:0000123  |  Nephritis  |  1
HP:0000508  |  Drooping upper eyelid  |  1
HP:0006744  |  Adrenal carcinoma  |  1
HP:0000793  |  Membranoproliferative glomerulonephritis  |  1
HP:0001298  |  Encephalopathy  |  1
HP:0002960  |  Autoimmune condition  |  1
HP:0003689  |  Multiple mtDNA deletions  |  1
HP:0002913  |  Myoglobinuria  |  1
HP:0006466  |  Ankle contracture  |  1
HP:0100279  |  Ulcerative colitis  |  1
HP:0000211  |  Trismus  |  1
HP:0005584  |  Renal cell carcinoma  |  1
HP:0011945  |  Cryptogenic organizing pneumonia  |  1
HP:0002608  |  Celiac disease  |  1
HP:0007824  |  Total ophthalmoplegia  |  1
HP:0100758  |  Gangrene  |  1
HP:0100533  |  Ocular inflammation  |  1
HP:0004836  |  Acute promyelocytic leukemia  |  1
HP:0002036  |  Hiatus hernia  |  1
HP:0001639  |  Hypertrophic cardiomyopathy  |  1
HP:0006562  |  Viral hepatitis  |  1
HP:0100033  |  Tic disorder  |  1
HP:0002273  |  Tetraparesis  |  1
HP:0001371  |  Flexion contractures of joints  |  1
HP:0002894  |  Neoplasia of the pancreas  |  1
HP:0005506  |  Chronic myeloid leukemia  |  1
HP:0005952  |  Decreased lung function  |  1
HP:0012114  |  Endometrial carcinoma  |  1
HP:0003774  |  End-stage renal failure  |  1
HP:0003202  |  Neurogenic muscle atrophy, especially in the lower limbs  |  1
HP:0004349  |  Reduced bone mineral density  |  1
HP:0001907  |  Thromboembolic disease  |  1
HP:0002721  |  Immunodeficiency  |  1
HP:0030078  |  Lung adenocarcinoma  |  1
HP:0003072  |  Hypercalcemia  |  1
Disease ID 493
Disease myositis
Manually Symptom
UMLS  | Name(Total Manually Symptoms:20)
C2707258  |  infections
C2697391  |  rheumatoid arthritis
C1962971  |  myocarditis
C0748159  |  pulmonary involvement
C0746787  |  neck cancer
C0741885  |  occult malignancy
C0410000  |  overlap syndrome
C0206062  |  interstitial lung disease
C0162323  |  polyarthritis
C0152025  |  polyneuropathy
C0085434  |  bacillary angiomatosis
C0038013  |  ankylosing spondylitis
C0035435  |  rheumatic diseases
C0034372  |  quadriplegia
C0027121  |  muscle inflammation
C0026896  |  myasthenia gravis
C0011849  |  diabetes mellitus
C0011168  |  dysphagia
C0009782  |  connective tissue disorder
C0006663  |  calcinosis
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:9)
C0004093  |  weakness  |  7
C0410000  |  overlap syndrome  |  5
C0003873  |  rheumatoid arthritis  |  4
C0206062  |  interstitial lung disease  |  3
C0011168  |  dysphagia  |  3
C0026848  |  myopathy  |  3
C0027059  |  myocarditis  |  2
C0027121  |  muscle inflammation  |  1
C0021311  |  infections  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
Text Mining Genotype(Total 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:1)
HP ID HP Name MP ID MP Name Annotation
HP:0003701Proximal muscle weaknessMP:0000748progressive muscle weaknessincreasing loss of muscle strength over time
Mapped by homologous gene(Total Items:2)
HP ID HP Name MP ID MP Name Annotation
HP:0100614MyositisMP:0011635abnormal mitochondrial crista morphologyAny of the inward folds of the mitochondrial inner membrane; crista number, extent, and shape differ in mitochondria from different tissues and organisms; crista appear to be devices for increasing the surface area of the mitochondrial inner membrane, whe
HP:0003701Proximal muscle weaknessMP:0020329decreased capillary densityreduction in the number of capillaries in a given cross-sectional area of a tissue
Disease ID 493
Disease myositis
Case(Waiting for update.)