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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine



   lupus erythematosus
  

Disease ID 804
Disease lupus erythematosus
Definition

What is lupus?

Lupus is an autoimmune disease. This means that your immune system attacks healthy cells and tissues by mistake. This can damage many parts of the body, including the joints, skin, kidneys, heart, lungs, blood vessels, and brain.

There are several kinds of lupus

  • Systemic lupus erythematosus (SLE) is the most common type. It can be mild or severe, and can affect many parts of the body.
  • Discoid lupus causes a red rash that doesn't go away
  • Subacute cutaneous lupus causes sores after being out in the sun
  • Drug-induced lupus is caused by certain medicines. It usually goes away when you stop taking the medicine.
  • Neonatal lupus, which is rare, affects newborns. It is probably caused by certain antibodies from the mother.

Who gets lupus?

Anyone can get lupus, but women are most at risk. Lupus is two to three times more common in African American women than in Caucasian women. It's also more common in Hispanic, Asian, and Native American women. African American and Hispanic women are more likely to have severe forms of lupus.

What causes lupus?

The cause of lupus is not known.

What are the symptoms of lupus?

Lupus can have many symptoms, and they differ from person to person. Some of the more common ones are

  • Pain or swelling in joints
  • Muscle pain
  • Fever with no known cause
  • Red rashes, most often on the face (also called the "butterfly rash")
  • Chest pain when taking a deep breath
  • Hair loss
  • Pale or purple fingers or toes
  • Sensitivity to the sun
  • Swelling in legs or around eyes
  • Mouth ulcers
  • Swollen glands
  • Feeling very tired

Symptoms may come and go. When you are having symptoms, it is called a flare. Flares can range from mild to severe. New symptoms may appear at any time.

How do I know if I have lupus?

There is no single test to diagnose lupus, and it's often mistaken for other diseases. So it may take months or years for a doctor to diagnose it. Your doctor may use many tools to make a diagnosis:

  • Medical history
  • Complete exam
  • Blood tests
  • Skin biopsy (looking at skin samples under a microscope)
  • Kidney biopsy (looking at tissue from your kidney under a microscope)

What are the treatments for lupus?

There is no cure for lupus, but medicines and lifestyle changes can help control it.

People with lupus often need to see different doctors. You will have a primary care doctor and a rheumatologist (a doctor who specializes in the diseases of joints and muscles). Which other specialists you see depends on how lupus affects your body. For example, if lupus damages your heart or blood vessels, you would see a cardiologist.

Your primary care doctor should coordinate care between your different health care providers and treat other problems as they come up. Your doctor will develop a treatment plan to fit your needs. You and your doctor should review the plan often to be sure it is working. You should report new symptoms to your doctor right away so that your treatment plan can be changed if needed.

The goals of the treatment plan are to

  • Prevent flares
  • Treat flares when they occur
  • Reduce organ damage and other problems

Treatments may include drugs to

  • Reduce swelling and pain
  • Prevent or reduce flares
  • Help the immune system
  • Reduce or prevent damage to joints
  • Balance the hormones

Besides taking medicines for lupus, you may need to take medicines for problems that are related to lupus such as high cholesterol, high blood pressure, or infection.

Alternative treatments are those that are not part of standard treatment. At this time, no research shows that alternative medicine can treat lupus. Some alternative or complementary approaches may help you cope or reduce some of the stress associated with living with a chronic illness. You should talk to your doctor before trying any alternative treatments.

How can I cope with lupus?

It is important to take an active role in your treatment. It helps to learn more about lupus - being able to spot the warning signs of a flare can help you prevent the flare or make the symptoms less severe.

It is also important to find ways to cope with the stress of having lupus. Exercising and finding ways to relax may make it easier for you to cope. A good support system can also help.

NIH: National Institute of Arthritis and Musculoskeletal and Skin Diseases


Synonym
le - lupus erythematosus
lupus erythematosus (disorder)
lupus erythematosus nos
lupus erythematosus nos (disorder)
DOID
UMLS
C0409974
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:367)
C0027697  |  nephritis  |  32
C0004153  |  atherosclerosis  |  29
C0024143  |  lupus nephritis  |  27
C0085278  |  antiphospholipid syndrome  |  21
C0042384  |  vasculitis  |  19
C0040034  |  thrombocytopenia  |  16
C0042373  |  vascular disease  |  13
C0003864  |  arthritis  |  13
C0020538  |  hypertension  |  11
C0034150  |  purpura  |  10
C0040053  |  thrombosis  |  9
C0007222  |  cardiovascular disease  |  9
C0022658  |  renal disease  |  9
C0042769  |  virus infection  |  9
C0033975  |  psychosis  |  9
C0034155  |  thrombotic thrombocytopenic purpura  |  8
C0017658  |  glomerulonephritis  |  8
C0011570  |  depression  |  8
C0002871  |  anemia  |  7
C0021053  |  immune disease  |  6
C0027051  |  myocardial infarction  |  6
C0026896  |  myasthenia gravis  |  6
C0948265  |  metabolic syndrome  |  6
C0020542  |  pulmonary hypertension  |  6
C0027051  |  myocardial infarct  |  6
C0041296  |  tuberculosis  |  6
C0003873  |  rheumatoid arthritis  |  6
C0022658  |  nephropathy  |  6
C0162855  |  mucinosis  |  5
C0006663  |  calcinosis  |  5
C0027121  |  myositis  |  5
C0011603  |  dermatitis  |  5
C0021847  |  intestinal pseudo-obstruction  |  4
C0007137  |  squamous cell carcinoma  |  4
C0030305  |  pancreatitis  |  4
C0014544  |  epilepsy  |  4
C0442874  |  neuropathy  |  4
C0002871  |  anaemia  |  4
C0019360  |  zoster  |  4
C0026946  |  fungal infection  |  4
C0021831  |  enteropathy  |  4
C0032285  |  pneumonia  |  4
C0002874  |  aplastic anemia  |  4
C0024141  |  systemic lupus erythematosus  |  4
C0004030  |  aspergillosis  |  4
C0003467  |  anxiety  |  4
C0024299  |  lymphoma  |  4
C0010346  |  crohn's disease  |  4
C0019360  |  herpes zoster  |  4
C0035309  |  retinopathy  |  4
C0019163  |  hepatitis b  |  4
C0031117  |  peripheral neuropathy  |  4
C0024291  |  hemophagocytic syndrome  |  4
C0027947  |  neutropenia  |  4
C0014742  |  erythema multiforme  |  4
C0021400  |  influenza  |  4
C0155626  |  acute myocardial infarction  |  4
C0003486  |  aortic aneurysm  |  3
C0019158  |  hepatitis  |  3
C0001339  |  acute pancreatitis  |  3
C0024115  |  lung disease  |  3
C1527336  |  sjogren's syndrome  |  3
C0033680  |  protein-losing enteropathy  |  3
C0024312  |  lymphopenia  |  3
C0035078  |  renal failure  |  3
C0026975  |  myelitis  |  3
C0001815  |  myelofibrosis  |  3
C0009782  |  connective tissue disease  |  3
C0042870  |  vitamin d deficiency  |  3
C0015230  |  rash  |  3
C0042870  |  vitamin d defic  |  3
C0026654  |  moyamoya syndrome  |  3
C0007642  |  cellulitis  |  3
C0040128  |  thyroid disease  |  3
C0034735  |  raynaud's phenomenon  |  3
C0011847  |  diabetes  |  3
C0022735  |  klinefelter's syndrome  |  3
C0026654  |  moyamoya  |  3
C0270612  |  leukoencephalopathy  |  3
C0011849  |  diabetes mellitus  |  3
C0027873  |  neuromyelitis optica  |  3
C0010068  |  coronary artery disease  |  3
C0039263  |  takayasu's arteritis  |  2
C0004096  |  asthma  |  2
C0026764  |  multiple myeloma  |  2
C0032285  |  pneumonitis  |  2
C0030326  |  panniculitis  |  2
C0031117  |  peripheral neuropathies  |  2
C0600260  |  obstructive pulmonary disease  |  2
C0149931  |  migraine  |  2
C0002880  |  autoimmune hemolytic anemia  |  2
C0022116  |  ischemia  |  2
C0022661  |  end-stage renal disease  |  2
C1704275  |  pyomyositis  |  2
C0035302  |  retinal artery occlusion  |  2
C0000786  |  miscarriage  |  2
C0006666  |  calciphylaxis  |  2
C0035333  |  retinitis  |  2
C0022658  |  kidney disease  |  2
C0206062  |  interstitial lung disease  |  2
C1619734  |  pulmonary arterial hypertension  |  2
C0004623  |  bacterial infection  |  2
C0020455  |  hypergammaglobulinemia  |  2
C0042373  |  vascular diseases  |  2
C0032326  |  pneumothorax  |  2
C0022661  |  chronic kidney disease  |  2
C0241910  |  autoimmune hepatitis  |  2
C0852949  |  arterial disease  |  2
C0151740  |  intracranial hypertension  |  2
C0026272  |  mixed connective tissue disease  |  2
C0039614  |  tetanus  |  2
C0038325  |  stevens-johnson syndrome  |  2
C0021655  |  insulin resistance syndrome  |  2
C0009319  |  colitis  |  2
C0034902  |  pure red cell aplasia  |  2
C0085278  |  anti-phospholipid syndrome  |  2
C0011644  |  scleroderma  |  2
C0025289  |  meningitis  |  2
C0024115  |  pulmonary disease  |  2
C0040100  |  thymoma  |  2
C1704436  |  peripheral arterial disease  |  2
C0026946  |  fungal infections  |  2
C0026764  |  myeloma  |  2
C0085278  |  antiphospholipid antibody syndrome  |  2
C0024314  |  lymphoproliferative disorder  |  2
C0007177  |  cardiac tamponade  |  2
C0032231  |  pleuritis  |  2
C0014306  |  enophthalmos  |  2
C0037198  |  sinus thrombosis  |  2
C0004623  |  bacterial infections  |  2
C0011615  |  atopic dermatitis  |  2
C0003504  |  aortic regurgitation  |  2
C0024117  |  chronic obstructive pulmonary disease  |  2
C0272242  |  complement deficiency  |  2
C0032285  |  pneumoniae  |  2
C0023895  |  liver disease  |  2
C0033860  |  psoriasis  |  2
C0002878  |  hemolytic anemia  |  2
C0017661  |  iga nephropathy  |  2
C0021359  |  infertile  |  2
C0272126  |  evans syndrome  |  1
C0022660  |  acute renal failure  |  1
C0014070  |  encephalomyelitis  |  1
C0079731  |  b cell lymphoma  |  1
C0162566  |  porphyria cutanea tarda  |  1
C0032587  |  polyradiculoneuropathy  |  1
C0017668  |  focal segmental glomerulosclerosis  |  1
C0152026  |  retinal vasculitis  |  1
C0001430  |  adenoma  |  1
C0035328  |  retinal vein occlusion  |  1
C0031212  |  personality disorders  |  1
C0041321  |  miliary tuberculosis  |  1
C0178664  |  glomerulosclerosis  |  1
C0010414  |  cryptococcus neoformans  |  1
C0020676  |  hypothyroid  |  1
C0014175  |  endometriosis  |  1
C0021345  |  infectious mononucleosis  |  1
C0020502  |  hyperparathyroidism  |  1
C0030499  |  parasitic disease  |  1
C0007115  |  thyroid ca  |  1
C0026848  |  myopathy  |  1
C0878544  |  cardiomyopathy  |  1
C0079293  |  epidermolysis bullosa acquisita  |  1
C1527383  |  morphea  |  1
C1262481  |  eosinophilic gastroenteritis  |  1
C0001175  |  acquired immune deficiency  |  1
C0035579  |  hypovitaminosis d  |  1
C0549473  |  thyroid carcinoma  |  1
C0017605  |  angle closure glaucoma  |  1
C0035435  |  rheumatic disease  |  1
C0004943  |  behcet's disease  |  1
C0019196  |  hepatitis c  |  1
C0024314  |  lymphoproliferative disorders  |  1
C0314719  |  dry eye  |  1
C0393819  |  chronic inflammatory demyelinating polyradiculoneuropathy  |  1
C0020295  |  hydronephrosis  |  1
C0038362  |  stomatitis  |  1
C0010051  |  coronary aneurysm  |  1
C0040147  |  thyroiditis  |  1
C0007222  |  cardiovascular disorders  |  1
C0031069  |  familial mediterranean fever  |  1
C0085293  |  hepatitis e  |  1
C1263846  |  attention deficit hyperactivity disorder  |  1
C0012569  |  diplopia  |  1
C0035302  |  retinal artery occlusions  |  1
C0030807  |  pemphigus  |  1
C0027726  |  nephrotic syndrome  |  1
C0001815  |  bone marrow fibrosis  |  1
C0281658  |  primary intraocular lymphoma  |  1
C0023343  |  hansen's disease  |  1
C1290398  |  cerebral artery aneurysm  |  1
C0035258  |  restless legs syndrome (rls)  |  1
C0011608  |  dermatitis herpetiformis  |  1
C0018801  |  heart failure  |  1
C0022735  |  klinefelter syndrome  |  1
C0023860  |  listeria monocytogenes infection  |  1
C0003850  |  arteriosclerosis  |  1
C0085436  |  cryptococcal meningitis  |  1
C0007222  |  cardiovascular diseases  |  1
C0027721  |  minimal change nephropathy  |  1
C0014059  |  acute disseminated encephalomyelitis  |  1
C0033680  |  protein losing enteropathy  |  1
C0007193  |  dilated cardiomyopathies  |  1
C0024623  |  gastric cancer  |  1
C0012546  |  diphtheria  |  1
C0030354  |  papilloma  |  1
C0042373  |  vascular disorders  |  1
C0020503  |  secondary hyperparathyroidism  |  1
C0002878  |  haemolytic anaemia  |  1
C0206157  |  nemaline myopathy  |  1
C0041309  |  tuberculosis cutis  |  1
C0019069  |  hemophilia  |  1
C0013592  |  ectropion  |  1
C0034069  |  pulmonary fibrosis  |  1
C0036416  |  scleritis  |  1
C0019202  |  wilson's disease  |  1
C0021831  |  bowel disease  |  1
C0155357  |  posterior scleritis  |  1
C0022656  |  renal cortical necrosis  |  1
C0151311  |  cranial nerve palsy  |  1
C0034065  |  pulmonary embolism  |  1
C1510471  |  hypovitaminosis  |  1
C0020626  |  hypoparathyroidism  |  1
C0030499  |  parasitic diseases  |  1
C0018378  |  guillain-barre syndrome  |  1
C0023524  |  progressive multifocal leukoencephalopathy  |  1
C0019048  |  hemoglobinuria  |  1
C0023646  |  lichen planus  |  1
C0272286  |  immune thrombocytopenia  |  1
C0017601  |  glaucoma  |  1
C0007847  |  cervical cancer  |  1
C0023890  |  liver cirrhosis  |  1
C0751878  |  cns vasculitis  |  1
C0025309  |  meningoencephalitis  |  1
C0920350  |  autoimmune thyroiditis  |  1
C0679466  |  cognitive deficits  |  1
C0010068  |  coronary heart disease  |  1
C0041296  |  mycobacterium tuberculosis infection  |  1
C0032305  |  pneumocystis  |  1
C0043092  |  wegener granulomatosis  |  1
C0023895  |  liver diseases  |  1
C0018784  |  sensorineural hearing loss  |  1
C0302592  |  cervical ca  |  1
C0040128  |  thyroid diseases  |  1
C0038220  |  status epilepticus  |  1
C0031046  |  pericarditis  |  1
C0003874  |  septic arthritis  |  1
C0006625  |  cachexia  |  1
C0087086  |  thrombi  |  1
C0032305  |  pneumocystis jiroveci pneumonia  |  1
C0035078  |  kidney failure  |  1
C0553723  |  cutaneous squamous cell carcinoma  |  1
C0007688  |  central retinal artery occlusion  |  1
C0018799  |  heart disease  |  1
C0000889  |  acanthosis nigricans  |  1
C0019360  |  herpes zoster infection  |  1
C0026848  |  myopathies  |  1
C0029134  |  optic neuritis  |  1
C0026986  |  myelodysplastic syndrome  |  1
C0276721  |  phaeohyphomycosis  |  1
C0032708  |  porphyria  |  1
C0020540  |  malignant hypertension  |  1
C0017665  |  membranous glomerulonephritis  |  1
C0752124  |  spinocerebellar ataxia type 6  |  1
C0162299  |  thyroid cyst  |  1
C0002453  |  amenorrhea  |  1
C0281963  |  red cell aplasia  |  1
C0206674  |  villous adenoma  |  1
C0019348  |  herpes simplex infection  |  1
C0001175  |  acquired immune deficiency syndrome  |  1
C0034012  |  delayed puberty  |  1
C0023890  |  cirrhosis  |  1
C0024205  |  lymphadenitis  |  1
C0281658  |  intraocular lymphoma  |  1
C0032269  |  streptococcus pneumoniae infection  |  1
C0085273  |  parvovirus b19 infection  |  1
C0036202  |  sarcoidosis  |  1
C0002895  |  sickle cell disease  |  1
C0002170  |  alopecia  |  1
C0017160  |  gastroenteritis  |  1
C0026718  |  mucormycosis  |  1
C0026946  |  mycosis  |  1
C0014121  |  infective endocarditis  |  1
C0014038  |  encephalitis  |  1
C0027813  |  neuritis  |  1
C0339962  |  pulmonary mucormycosis  |  1
C0242584  |  autoimmune thrombocytopenia  |  1
C0001175  |  acquired immune deficiency syndrome (aids)  |  1
C0015458  |  parry-romberg syndrome  |  1
C0010692  |  cystitis  |  1
C0007766  |  cranial aneurysm  |  1
C0027709  |  nephrocalcinosis  |  1
C0002874  |  aplastic anaemia  |  1
C0007766  |  intracranial aneurysm  |  1
C0031099  |  periodontitis  |  1
C0206093  |  primitive neuroectodermal tumor  |  1
C0009782  |  connective tissue diseases  |  1
C1565489  |  renal insufficiency  |  1
C0024790  |  paroxysmal nocturnal hemoglobinuria  |  1
C0024894  |  mastitis  |  1
C0014868  |  esophagitis  |  1
C0021359  |  infertility  |  1
C0001126  |  renal tubular acidosis  |  1
C0042109  |  urticaria  |  1
C0041188  |  tropical pyomyositis  |  1
C0151744  |  myocardial ischemia  |  1
C0033845  |  idiopathic intracranial hypertension  |  1
C0007682  |  cns disease  |  1
C0010051  |  coronary aneurysms  |  1
C0021390  |  inflammatory bowel disease  |  1
C0004134  |  ataxia  |  1
C0033687  |  proteinuria  |  1
C0677607  |  hashimoto's thyroiditis  |  1
C0014118  |  endocarditis  |  1
C0730306  |  ocular lymphoma  |  1
C0018552  |  hamartoma  |  1
C0149530  |  congenital heart block  |  1
C0032305  |  pneumocystis carinii pneumonia  |  1
C1145670  |  respiratory failure  |  1
C0235618  |  proliferative glomerulonephritis  |  1
C0006142  |  breast cancer  |  1
C0031039  |  pericardial effusion  |  1
C0206178  |  cmv retinitis  |  1
C0029456  |  osteoporosis  |  1
C0022408  |  arthropathy  |  1
C0276088  |  escherichia coli septicemia  |  1
C0020598  |  hypoglycemia  |  1
C0020676  |  hypothyroidism  |  1
C0042900  |  vitiligo  |  1
C0007758  |  cerebellar ataxia  |  1
C0162872  |  thoracic aortic aneurysm  |  1
C0042594  |  vestibular disorders  |  1
C0012813  |  diverticulitis  |  1
C0162429  |  malnutrition  |  1
C0152966  |  pneumococcal septicaemia  |  1
C0238124  |  necrotizing fasciitis  |  1
C0238463  |  papillary thyroid carcinoma  |  1
C0010054  |  coronary atherosclerosis  |  1
C0026948  |  mycosis fungoides  |  1
C0019348  |  herpes simplex  |  1
C0042109  |  urticarial  |  1
C0023418  |  leukemia  |  1
C0041318  |  tuberculous meningitis  |  1
C0035435  |  rheumatic diseases  |  1
C0011633  |  dermatomyositis  |  1
C0002895  |  sickle-cell disease  |  1
C0043117  |  immune thrombocytopenic purpura  |  1
C0010481  |  cushing's syndrome  |  1
C0041408  |  turner syndrome  |  1
C0003486  |  aortic aneurysms  |  1
C0151436  |  leukocytoclastic vasculitis  |  1
C0038463  |  strongyloidiasis  |  1
C0085292  |  stiff-person syndrome  |  1
C0519030  |  klebsiella pneumonia  |  1
C0085278  |  anti-phospholipid antibody syndrome  |  1
C0041328  |  renal tuberculosis  |  1
C0024299  |  lymphomas  |  1
C1527336  |  sjogren syndrome  |  1
C0031090  |  periodontal disease  |  1
C0005586  |  bipolar affective disorder  |  1
C0042373  |  vascular disorder  |  1
C0037928  |  myelopathy  |  1
C0026985  |  myelodysplasia  |  1
C0021345  |  mononucleosis  |  1
C0033975  |  psychotic disorder  |  1
C0002173  |  follicular mucinosis  |  1
C0524812  |  intracranial hypotension  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:24)
11277  |  TREX1  |  UniProtKB-KW;GHR
7128  |  TNFAIP3  |  GHR
6775  |  STAT4  |  UniProtKB-KW;GHR
1493  |  CTLA4  |  UniProtKB-KW
26191  |  PTPN22  |  GHR
1401  |  CRP  |  GHR
7100  |  TLR5  |  UniProtKB-KW;GHR
4058  |  LTK  |  UniProtKB-KW
10125  |  RASGRP1  |  UniProtKB-KW
4688  |  NCF2  |  GHR
7292  |  TNFSF4  |  UniProtKB-KW
1380  |  CR2  |  UniProtKB-KW;GHR
3663  |  IRF5  |  UniProtKB-KW;GHR
720  |  C4A  |  UniProtKB-KW;GHR
2547  |  XRCC6  |  UniProtKB-KW
2213  |  FCGR2B  |  UniProtKB-KW;GHR
8737  |  RIPK1  |  GHR
3684  |  ITGAM  |  UniProtKB-KW;GHR
55024  |  BANK1  |  GHR
5133  |  PDCD1  |  UniProtKB-KW;GHR
721  |  C4B  |  UniProtKB-KW
1776  |  DNASE1L3  |  GHR
7520  |  XRCC5  |  UniProtKB-KW
1773  |  DNASE1  |  GHR
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:71)
712  |  C1QA  |  CIPHER
720  |  C4A  |  CIPHER
721  |  C4B  |  CIPHER
6347  |  CCL2  |  CIPHER
6352  |  CCL5  |  CIPHER
729230  |  CCR2  |  CIPHER
1234  |  CCR5  |  CIPHER
952  |  CD38  |  CIPHER
959  |  CD40LG  |  CIPHER
971  |  CD72  |  CIPHER
4261  |  CIITA  |  CIPHER
1378  |  CR1  |  CIPHER
1380  |  CR2  |  CIPHER
1493  |  CTLA4  |  CIPHER
1773  |  DNASE1  |  CIPHER
1777  |  DNASE2  |  CIPHER
1786  |  DNMT1  |  CIPHER
1956  |  EGFR  |  CIPHER
356  |  FASLG  |  CIPHER
2204  |  FCAR  |  CIPHER
2212  |  FCGR2A  |  CIPHER
2213  |  FCGR2B  |  CIPHER
2214  |  FCGR3A  |  CIPHER
2215  |  FCGR3B  |  CIPHER
55340  |  GIMAP5  |  CIPHER
3059  |  HCLS1  |  CIPHER
3105  |  HLA-A  |  CIPHER
3106  |  HLA-B  |  CIPHER
3107  |  HLA-C  |  CIPHER
3108  |  HLA-DMA  |  CIPHER
3109  |  HLA-DMB  |  CIPHER
3117  |  HLA-DQA1  |  CIPHER
3119  |  HLA-DQB1  |  CIPHER
3123  |  HLA-DRB1  |  CIPHER
3306  |  HSPA2  |  CIPHER
3439  |  IFNA1  |  CIPHER
3459  |  IFNGR1  |  CIPHER
3460  |  IFNGR2  |  CIPHER
3586  |  IL10  |  CIPHER
3552  |  IL1A  |  CIPHER
3557  |  IL1RN  |  CIPHER
3569  |  IL6  |  CIPHER
3663  |  IRF5  |  CIPHER
3821  |  KLRC1  |  CIPHER
4049  |  LTA  |  CIPHER
4153  |  MBL2  |  CIPHER
10461  |  MERTK  |  CIPHER
100507436  |  MICA  |  CIPHER
4277  |  MICB  |  CIPHER
4282  |  MIF  |  CIPHER
4846  |  NOS3  |  CIPHER
2908  |  NR3C1  |  CIPHER
22854  |  NTNG1  |  CIPHER
142  |  PARP1  |  CIPHER
5133  |  PDCD1  |  CIPHER
5743  |  PTGS2  |  CIPHER
26191  |  PTPN22  |  CIPHER
861  |  RUNX1  |  CIPHER
6583  |  SLC22A4  |  CIPHER
6696  |  SPP1  |  CIPHER
387082  |  SUMO4  |  CIPHER
6890  |  TAP1  |  CIPHER
6891  |  TAP2  |  CIPHER
7100  |  TLR5  |  CIPHER
54106  |  TLR9  |  CIPHER
7124  |  TNF  |  CIPHER
23495  |  TNFRSF13B  |  CIPHER
7133  |  TNFRSF1B  |  CIPHER
8741  |  TNFSF13  |  CIPHER
7172  |  TPMT  |  CIPHER
7297  |  TYK2  |  CIPHER
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:517)
2  |  A2M  |  1.294  |  DISEASES
130013  |  ACMSD  |  1.011  |  DISEASES
60  |  ACTB  |  1.582  |  DISEASES
94  |  ACVRL1  |  1.205  |  DISEASES
100  |  ADA  |  1.331  |  DISEASES
11093  |  ADAMTS13  |  3.495  |  DISEASES
103  |  ADAR  |  1.869  |  DISEASES
79747  |  ADGB  |  2.114  |  DISEASES
9370  |  ADIPOQ  |  1.745  |  DISEASES
340351  |  AGBL3  |  2.245  |  DISEASES
9447  |  AIM2  |  3.359  |  DISEASES
64400  |  AKTIP  |  1.158  |  DISEASES
91526  |  ANKRD44  |  1.993  |  DISEASES
57182  |  ANKRD50  |  1.275  |  DISEASES
23294  |  ANKS1A  |  1.775  |  DISEASES
302  |  ANXA2  |  2.274  |  DISEASES
55937  |  APOM  |  1.376  |  DISEASES
100505854  |  APTR  |  1.031  |  DISEASES
361  |  AQP4  |  2.659  |  DISEASES
1388  |  ATF6B  |  1.156  |  DISEASES
9474  |  ATG5  |  1.922  |  DISEASES
551  |  AVP  |  1.034  |  DISEASES
567  |  B2M  |  3.163  |  DISEASES
29086  |  BABAM1  |  2.742  |  DISEASES
55024  |  BANK1  |  4.574  |  DISEASES
57673  |  BEND3  |  1.056  |  DISEASES
632  |  BGLAP  |  1.532  |  DISEASES
151888  |  BTLA  |  1.783  |  DISEASES
56244  |  BTNL2  |  1.661  |  DISEASES
10917  |  BTNL3  |  1.534  |  DISEASES
79908  |  BTNL8  |  1.365  |  DISEASES
153579  |  BTNL9  |  1.119  |  DISEASES
712  |  C1QA  |  3.947  |  DISEASES
714  |  C1QC  |  3.547  |  DISEASES
716  |  C1S  |  4.37  |  DISEASES
720  |  C4A  |  5.285  |  DISEASES
721  |  C4B  |  4.961  |  DISEASES
728  |  C5AR1  |  2.278  |  DISEASES
10665  |  C6orf10  |  1.648  |  DISEASES
773  |  CACNA1A  |  1.02  |  DISEASES
801  |  CALM1  |  1.244  |  DISEASES
811  |  CALR  |  3.458  |  DISEASES
820  |  CAMP  |  2.055  |  DISEASES
834  |  CASP1  |  2.886  |  DISEASES
841  |  CASP8  |  1.971  |  DISEASES
831  |  CAST  |  1.395  |  DISEASES
339965  |  CCDC158  |  1.09  |  DISEASES
6364  |  CCL20  |  1.395  |  DISEASES
6349  |  CCL3L1  |  1.737  |  DISEASES
388372  |  CCL4L1  |  1.644  |  DISEASES
9034  |  CCRL2  |  1.102  |  DISEASES
977  |  CD151  |  1.284  |  DISEASES
9332  |  CD163  |  1.766  |  DISEASES
930  |  CD19  |  4.636  |  DISEASES
911  |  CD1C  |  2.245  |  DISEASES
912  |  CD1D  |  3.515  |  DISEASES
914  |  CD2  |  2.202  |  DISEASES
51744  |  CD244  |  2.88  |  DISEASES
919  |  CD247  |  3.432  |  DISEASES
29126  |  CD274  |  2.24  |  DISEASES
146722  |  CD300LF  |  1.967  |  DISEASES
958  |  CD40  |  4.609  |  DISEASES
959  |  CD40LG  |  6.728  |  DISEASES
960  |  CD44  |  2.722  |  DISEASES
962  |  CD48  |  2.538  |  DISEASES
921  |  CD5  |  3.803  |  DISEASES
966  |  CD59  |  2.046  |  DISEASES
974  |  CD79B  |  1.872  |  DISEASES
9308  |  CD83  |  2.215  |  DISEASES
942  |  CD86  |  4.147  |  DISEASES
1038  |  CDR1  |  4.045  |  DISEASES
1041  |  CDSN  |  5.071  |  DISEASES
1058  |  CENPA  |  1.192  |  DISEASES
1059  |  CENPB  |  3.384  |  DISEASES
401541  |  CENPP  |  1.412  |  DISEASES
55166  |  CENPQ  |  1.188  |  DISEASES
629  |  CFB  |  2.435  |  DISEASES
3075  |  CFH  |  2.01  |  DISEASES
10877  |  CFHR4  |  1.375  |  DISEASES
3426  |  CFI  |  1.21  |  DISEASES
23274  |  CLEC16A  |  1.581  |  DISEASES
388512  |  CLEC17A  |  1.496  |  DISEASES
170482  |  CLEC4C  |  3.55  |  DISEASES
146223  |  CMTM4  |  1.334  |  DISEASES
10695  |  CNPY3  |  1.222  |  DISEASES
124817  |  CNTD1  |  1.45  |  DISEASES
22796  |  COG2  |  1.775  |  DISEASES
1308  |  COL17A1  |  1.984  |  DISEASES
10087  |  COL4A3BP  |  1.203  |  DISEASES
1378  |  CR1  |  4.619  |  DISEASES
1380  |  CR2  |  2.665  |  DISEASES
1385  |  CREB1  |  1.133  |  DISEASES
1435  |  CSF1  |  2.386  |  DISEASES
1471  |  CST3  |  1.126  |  DISEASES
1524  |  CX3CR1  |  1.404  |  DISEASES
6387  |  CXCL12  |  2.379  |  DISEASES
4283  |  CXCL9  |  2.861  |  DISEASES
2833  |  CXCR3  |  3.498  |  DISEASES
7852  |  CXCR4  |  1.978  |  DISEASES
1536  |  CYBB  |  1.524  |  DISEASES
1589  |  CYP21A2  |  1.255  |  DISEASES
1557  |  CYP2C19  |  1.455  |  DISEASES
1565  |  CYP2D6  |  1.681  |  DISEASES
115265  |  DDIT4L  |  1.008  |  DISEASES
51428  |  DDX41  |  5.672  |  DISEASES
23586  |  DDX58  |  2.133  |  DISEASES
79947  |  DHDDS  |  1.161  |  DISEASES
1660  |  DHX9  |  1.773  |  DISEASES
8701  |  DNAH11  |  1.674  |  DISEASES
1786  |  DNMT1  |  3.471  |  DISEASES
1789  |  DNMT3B  |  1.444  |  DISEASES
1791  |  DNTT  |  1.437  |  DISEASES
22845  |  DOLK  |  1.173  |  DISEASES
29952  |  DPP7  |  1.17  |  DISEASES
1805  |  DPT  |  1.072  |  DISEASES
54935  |  DUSP23  |  1.209  |  DISEASES
1847  |  DUSP5  |  3.12  |  DISEASES
1850  |  DUSP8  |  1.182  |  DISEASES
1854  |  DUT  |  1.649  |  DISEASES
1781  |  DYNC1I2  |  2.244  |  DISEASES
1906  |  EDN1  |  1.241  |  DISEASES
163126  |  EID2  |  1.37  |  DISEASES
953  |  ENTPD1  |  1.107  |  DISEASES
2086  |  ERV3-1  |  1.474  |  DISEASES
30816  |  ERVW-1  |  2.339  |  DISEASES
2100  |  ESR2  |  1.608  |  DISEASES
2113  |  ETS1  |  3.103  |  DISEASES
5394  |  EXOSC10  |  3.219  |  DISEASES
5393  |  EXOSC9  |  1.263  |  DISEASES
346007  |  EYS  |  1.162  |  DISEASES
2160  |  F11  |  1.598  |  DISEASES
2152  |  F3  |  5.114  |  DISEASES
2153  |  F5  |  1.662  |  DISEASES
2155  |  F7  |  2.174  |  DISEASES
2157  |  F8  |  2.852  |  DISEASES
338811  |  FAM19A2  |  1.506  |  DISEASES
149297  |  FAM78B  |  1.088  |  DISEASES
355  |  FAS  |  3.764  |  DISEASES
356  |  FASLG  |  3.974  |  DISEASES
2205  |  FCER1A  |  1.158  |  DISEASES
2209  |  FCGR1A  |  2.905  |  DISEASES
2213  |  FCGR2B  |  5.123  |  DISEASES
2214  |  FCGR3A  |  3.486  |  DISEASES
9873  |  FCHSD2  |  2.159  |  DISEASES
2219  |  FCN1  |  2.475  |  DISEASES
115352  |  FCRL3  |  3.501  |  DISEASES
2312  |  FLG  |  1.545  |  DISEASES
23768  |  FLRT2  |  1.707  |  DISEASES
2323  |  FLT3LG  |  1.139  |  DISEASES
2290  |  FOXG1  |  2.423  |  DISEASES
2302  |  FOXJ1  |  1.647  |  DISEASES
50943  |  FOXP3  |  4.823  |  DISEASES
2533  |  FYB  |  1.09  |  DISEASES
2534  |  FYN  |  1.841  |  DISEASES
10146  |  G3BP1  |  1.788  |  DISEASES
1647  |  GADD45A  |  1.028  |  DISEASES
60674  |  GAS5  |  1.009  |  DISEASES
2621  |  GAS6  |  2.482  |  DISEASES
2625  |  GATA3  |  1.876  |  DISEASES
2737  |  GLI3  |  1.362  |  DISEASES
2800  |  GOLGA1  |  2.048  |  DISEASES
23015  |  GOLGA8A  |  1.61  |  DISEASES
29933  |  GPR132  |  2.3  |  DISEASES
2903  |  GRIN2A  |  2.684  |  DISEASES
2932  |  GSK3B  |  1.576  |  DISEASES
2962  |  GTF2F1  |  1.047  |  DISEASES
2969  |  GTF2I  |  1.554  |  DISEASES
9569  |  GTF2IRD1  |  1.889  |  DISEASES
3005  |  H1F0  |  3.716  |  DISEASES
3035  |  HARS  |  2.22  |  DISEASES
26762  |  HAVCR1  |  1.668  |  DISEASES
3039  |  HBA1  |  1.297  |  DISEASES
3052  |  HCCS  |  1.115  |  DISEASES
3055  |  HCK  |  1.042  |  DISEASES
9734  |  HDAC9  |  1.193  |  DISEASES
3009  |  HIST1H1B  |  1.359  |  DISEASES
8969  |  HIST1H2AG  |  1.331  |  DISEASES
8329  |  HIST1H2AI  |  1.331  |  DISEASES
8330  |  HIST1H2AK  |  1.201  |  DISEASES
8332  |  HIST1H2AL  |  1.331  |  DISEASES
8341  |  HIST1H2BN  |  2.272  |  DISEASES
8359  |  HIST1H4A  |  2.046  |  DISEASES
8366  |  HIST1H4B  |  2.046  |  DISEASES
8364  |  HIST1H4C  |  2.046  |  DISEASES
8360  |  HIST1H4D  |  2.045  |  DISEASES
8367  |  HIST1H4E  |  2.046  |  DISEASES
8361  |  HIST1H4F  |  2.046  |  DISEASES
8294  |  HIST1H4I  |  2.046  |  DISEASES
8363  |  HIST1H4J  |  2.046  |  DISEASES
8362  |  HIST1H4K  |  2.046  |  DISEASES
8368  |  HIST1H4L  |  2.046  |  DISEASES
8337  |  HIST2H2AA3  |  4.898  |  DISEASES
317772  |  HIST2H2AB  |  1.304  |  DISEASES
8338  |  HIST2H2AC  |  4.898  |  DISEASES
8349  |  HIST2H2BE  |  5.025  |  DISEASES
8370  |  HIST2H4A  |  2.046  |  DISEASES
554313  |  HIST2H4B  |  2.046  |  DISEASES
128312  |  HIST3H2BB  |  1.48  |  DISEASES
121504  |  HIST4H4  |  2.046  |  DISEASES
3105  |  HLA-A  |  3.145  |  DISEASES
3106  |  HLA-B  |  2.334  |  DISEASES
3107  |  HLA-C  |  1.095  |  DISEASES
3108  |  HLA-DMA  |  1.78  |  DISEASES
3109  |  HLA-DMB  |  1.434  |  DISEASES
3115  |  HLA-DPB1  |  2.578  |  DISEASES
3117  |  HLA-DQA1  |  3.244  |  DISEASES
3118  |  HLA-DQA2  |  1.699  |  DISEASES
3119  |  HLA-DQB1  |  2.786  |  DISEASES
3120  |  HLA-DQB2  |  2.774  |  DISEASES
3122  |  HLA-DRA  |  1.883  |  DISEASES
3123  |  HLA-DRB1  |  4.295  |  DISEASES
3127  |  HLA-DRB5  |  2.996  |  DISEASES
3135  |  HLA-G  |  1.976  |  DISEASES
3146  |  HMGB1  |  3.033  |  DISEASES
3151  |  HMGN2  |  2.687  |  DISEASES
3178  |  HNRNPA1  |  1.42  |  DISEASES
3181  |  HNRNPA2B1  |  2.51  |  DISEASES
220988  |  HNRNPA3  |  1.138  |  DISEASES
3240  |  HP  |  2.021  |  DISEASES
3320  |  HSP90AA1  |  2.257  |  DISEASES
3326  |  HSP90AB1  |  1.634  |  DISEASES
51182  |  HSPA14  |  1.162  |  DISEASES
3329  |  HSPD1  |  3.001  |  DISEASES
3339  |  HSPG2  |  3.827  |  DISEASES
3360  |  HTR4  |  1.217  |  DISEASES
3386  |  ICAM4  |  1.252  |  DISEASES
23308  |  ICOSLG  |  2.402  |  DISEASES
414328  |  IDNK  |  2.054  |  DISEASES
3428  |  IFI16  |  2.783  |  DISEASES
10561  |  IFI44  |  2.085  |  DISEASES
10964  |  IFI44L  |  2.995  |  DISEASES
2537  |  IFI6  |  1.547  |  DISEASES
3434  |  IFIT1  |  2.889  |  DISEASES
3437  |  IFIT3  |  1.849  |  DISEASES
3451  |  IFNA17  |  2.321  |  DISEASES
3440  |  IFNA2  |  2.023  |  DISEASES
3455  |  IFNAR2  |  2.179  |  DISEASES
3456  |  IFNB1  |  3.202  |  DISEASES
3459  |  IFNGR1  |  1.15  |  DISEASES
10320  |  IKZF1  |  2.948  |  DISEASES
22806  |  IKZF3  |  2.264  |  DISEASES
3586  |  IL10  |  5.31  |  DISEASES
3594  |  IL12RB1  |  1.399  |  DISEASES
3605  |  IL17A  |  4.784  |  DISEASES
112744  |  IL17F  |  2.001  |  DISEASES
29949  |  IL19  |  1.426  |  DISEASES
84639  |  IL1F10  |  1.604  |  DISEASES
50615  |  IL21R  |  2.788  |  DISEASES
50616  |  IL22  |  2.105  |  DISEASES
149233  |  IL23R  |  1.742  |  DISEASES
3559  |  IL2RA  |  2.649  |  DISEASES
133396  |  IL31RA  |  3.8  |  DISEASES
90865  |  IL33  |  1.402  |  DISEASES
3563  |  IL3RA  |  3.584  |  DISEASES
3608  |  ILF2  |  1.809  |  DISEASES
3609  |  ILF3  |  1.301  |  DISEASES
3635  |  INPP5D  |  1.86  |  DISEASES
3654  |  IRAK1  |  3.118  |  DISEASES
51135  |  IRAK4  |  2.474  |  DISEASES
3660  |  IRF2  |  1.23  |  DISEASES
3662  |  IRF4  |  2.711  |  DISEASES
3663  |  IRF5  |  5.738  |  DISEASES
3665  |  IRF7  |  3.77  |  DISEASES
10379  |  IRF9  |  1.458  |  DISEASES
9636  |  ISG15  |  2.844  |  DISEASES
3683  |  ITGAL  |  3.442  |  DISEASES
3684  |  ITGAM  |  3.853  |  DISEASES
3716  |  JAK1  |  1.589  |  DISEASES
3717  |  JAK2  |  1.033  |  DISEASES
3725  |  JUN  |  1.595  |  DISEASES
10945  |  KDELR1  |  1.056  |  DISEASES
23240  |  KIAA0922  |  1.334  |  DISEASES
3798  |  KIF5A  |  1.424  |  DISEASES
3802  |  KIR2DL1  |  2.061  |  DISEASES
3803  |  KIR2DL2  |  1.795  |  DISEASES
3804  |  KIR2DL3  |  1.841  |  DISEASES
3805  |  KIR2DL4  |  1.716  |  DISEASES
59349  |  KLHL12  |  1.699  |  DISEASES
55975  |  KLHL7  |  1.162  |  DISEASES
9622  |  KLK4  |  1.991  |  DISEASES
3821  |  KLRC1  |  1.996  |  DISEASES
3822  |  KLRC2  |  2.315  |  DISEASES
3824  |  KLRD1  |  1.563  |  DISEASES
3841  |  KPNA5  |  1.439  |  DISEASES
3895  |  KTN1  |  1.039  |  DISEASES
3903  |  LAIR1  |  2.779  |  DISEASES
3916  |  LAMP1  |  1.769  |  DISEASES
27040  |  LAT  |  1.247  |  DISEASES
81606  |  LBH  |  2.254  |  DISEASES
3932  |  LCK  |  2.654  |  DISEASES
84247  |  LDOC1L  |  1.243  |  DISEASES
3965  |  LGALS9  |  1.743  |  DISEASES
101927624  |  LINC01150  |  1.52  |  DISEASES
100885779  |  LINC-ROR  |  1.07  |  DISEASES
25802  |  LMOD1  |  1.302  |  DISEASES
4018  |  LPA  |  1.741  |  DISEASES
474354  |  LRRC18  |  2.245  |  DISEASES
55222  |  LRRC20  |  2.026  |  DISEASES
4049  |  LTA  |  2.624  |  DISEASES
4063  |  LY9  |  3.406  |  DISEASES
4067  |  LYN  |  3.692  |  DISEASES
388695  |  LYSMD1  |  2.087  |  DISEASES
4113  |  MAGEB2  |  1.198  |  DISEASES
11184  |  MAP4K1  |  1.235  |  DISEASES
5599  |  MAPK8  |  1.82  |  DISEASES
10747  |  MASP2  |  2.169  |  DISEASES
57506  |  MAVS  |  2.074  |  DISEASES
115004  |  MB21D1  |  1.726  |  DISEASES
4153  |  MBL2  |  3.411  |  DISEASES
4155  |  MBP  |  1.806  |  DISEASES
161357  |  MDGA2  |  1.733  |  DISEASES
23195  |  MDN1  |  1.054  |  DISEASES
4204  |  MECP2  |  2.289  |  DISEASES
79104  |  MEG8  |  1.175  |  DISEASES
100507436  |  MICA  |  1.78  |  DISEASES
407975  |  MIR17HG  |  1.002  |  DISEASES
4318  |  MMP9  |  2.249  |  DISEASES
4332  |  MNDA  |  2.492  |  DISEASES
4340  |  MOG  |  1.004  |  DISEASES
4439  |  MSH5  |  1.745  |  DISEASES
4524  |  MTHFR  |  1.892  |  DISEASES
8897  |  MTMR3  |  1.97  |  DISEASES
2475  |  MTOR  |  2.002  |  DISEASES
4599  |  MX1  |  3.801  |  DISEASES
4602  |  MYB  |  1.474  |  DISEASES
4609  |  MYC  |  1.623  |  DISEASES
4615  |  MYD88  |  3.057  |  DISEASES
4650  |  MYO9B  |  1.321  |  DISEASES
4688  |  NCF2  |  2.135  |  DISEASES
9436  |  NCR2  |  1.122  |  DISEASES
4772  |  NFATC1  |  1.092  |  DISEASES
4773  |  NFATC2  |  1.895  |  DISEASES
4803  |  NGF  |  1.411  |  DISEASES
54475  |  NLE1  |  2.694  |  DISEASES
22861  |  NLRP1  |  2.133  |  DISEASES
114548  |  NLRP3  |  2.615  |  DISEASES
4843  |  NOS2  |  1.043  |  DISEASES
4868  |  NPHS1  |  1.471  |  DISEASES
7827  |  NPHS2  |  1.386  |  DISEASES
4938  |  OAS1  |  2.576  |  DISEASES
4939  |  OAS2  |  2.028  |  DISEASES
4942  |  OAT  |  1.334  |  DISEASES
4948  |  OCA2  |  3.461  |  DISEASES
338662  |  OR8D4  |  2.026  |  DISEASES
5027  |  P2RX7  |  1.253  |  DISEASES
23569  |  PADI4  |  2.793  |  DISEASES
142  |  PARP1  |  1.542  |  DISEASES
64098  |  PARVG  |  1.01  |  DISEASES
5087  |  PBX1  |  1.624  |  DISEASES
5133  |  PDCD1  |  3.874  |  DISEASES
80380  |  PDCD1LG2  |  1.232  |  DISEASES
5143  |  PDE4C  |  1.367  |  DISEASES
57162  |  PELI1  |  1.451  |  DISEASES
5236  |  PGM1  |  1.182  |  DISEASES
5238  |  PGM3  |  1.277  |  DISEASES
57649  |  PHF12  |  1.11  |  DISEASES
57661  |  PHRF1  |  3.359  |  DISEASES
54872  |  PIGG  |  2.123  |  DISEASES
93183  |  PIGM  |  1.358  |  DISEASES
23556  |  PIGN  |  1.35  |  DISEASES
5293  |  PIK3CD  |  1.404  |  DISEASES
5294  |  PIK3CG  |  1.852  |  DISEASES
79837  |  PIP4K2C  |  1.421  |  DISEASES
59339  |  PLEKHA2  |  1.168  |  DISEASES
79666  |  PLEKHF2  |  1.176  |  DISEASES
5359  |  PLSCR1  |  1.798  |  DISEASES
29944  |  PNMA3  |  2.121  |  DISEASES
10623  |  POLR3C  |  1.397  |  DISEASES
5515  |  PPP2CA  |  2.516  |  DISEASES
639  |  PRDM1  |  2.638  |  DISEASES
56980  |  PRDM10  |  1.162  |  DISEASES
5580  |  PRKCD  |  1.475  |  DISEASES
5618  |  PRLR  |  2.455  |  DISEASES
5627  |  PROS1  |  1.642  |  DISEASES
11168  |  PSIP1  |  2.246  |  DISEASES
5696  |  PSMB8  |  1.428  |  DISEASES
5743  |  PTGS2  |  1.423  |  DISEASES
2185  |  PTK2B  |  1.468  |  DISEASES
26191  |  PTPN22  |  4.631  |  DISEASES
5788  |  PTPRC  |  3.133  |  DISEASES
54899  |  PXK  |  3.832  |  DISEASES
11264  |  PXMP4  |  1.125  |  DISEASES
149628  |  PYHIN1  |  2.864  |  DISEASES
5867  |  RAB4A  |  3.478  |  DISEASES
25780  |  RASGRP3  |  1.583  |  DISEASES
55225  |  RAVER2  |  1.269  |  DISEASES
27316  |  RBMX  |  2.355  |  DISEASES
54542  |  RC3H2  |  2.343  |  DISEASES
440163  |  RNASE13  |  1.2  |  DISEASES
79621  |  RNASEH2B  |  1.683  |  DISEASES
7732  |  RNF112  |  2.003  |  DISEASES
91445  |  RNF185  |  1.498  |  DISEASES
6086  |  RNY4  |  1.717  |  DISEASES
6097  |  RORC  |  1.253  |  DISEASES
80135  |  RPF1  |  1.737  |  DISEASES
6129  |  RPL7  |  2.499  |  DISEASES
79897  |  RPP21  |  1.214  |  DISEASES
6187  |  RPS2  |  3.183  |  DISEASES
6224  |  RPS20  |  1.048  |  DISEASES
6280  |  S100A9  |  1.48  |  DISEASES
6288  |  SAA1  |  1.974  |  DISEASES
1757  |  SARDH  |  3.052  |  DISEASES
9728  |  SECISBP2L  |  1.173  |  DISEASES
6401  |  SELE  |  3.397  |  DISEASES
5265  |  SERPINA1  |  2.531  |  DISEASES
1992  |  SERPINB1  |  1.689  |  DISEASES
5271  |  SERPINB8  |  1.588  |  DISEASES
462  |  SERPINC1  |  3.842  |  DISEASES
5345  |  SERPINF2  |  2.703  |  DISEASES
7536  |  SF1  |  1.184  |  DISEASES
4068  |  SH2D1A  |  1.365  |  DISEASES
117157  |  SH2D1B  |  1.554  |  DISEASES
9047  |  SH2D2A  |  1.331  |  DISEASES
59307  |  SIGIRR  |  2.745  |  DISEASES
6614  |  SIGLEC1  |  3.016  |  DISEASES
8778  |  SIGLEC5  |  1.501  |  DISEASES
114836  |  SLAMF6  |  3.83  |  DISEASES
57823  |  SLAMF7  |  2.288  |  DISEASES
6520  |  SLC3A2  |  2.039  |  DISEASES
9748  |  SLK  |  4.106  |  DISEASES
9887  |  SMG7  |  1.767  |  DISEASES
23583  |  SMUG1  |  1.43  |  DISEASES
26770  |  SNORD79  |  1.716  |  DISEASES
6625  |  SNRNP70  |  5.97  |  DISEASES
6628  |  SNRPB  |  3.532  |  DISEASES
8651  |  SOCS1  |  2.163  |  DISEASES
9021  |  SOCS3  |  1.126  |  DISEASES
10580  |  SORBS1  |  1.661  |  DISEASES
6667  |  SP1  |  1.337  |  DISEASES
6672  |  SP100  |  1.659  |  DISEASES
145946  |  SPATA8  |  2.08  |  DISEASES
26010  |  SPATS2L  |  1.002  |  DISEASES
6693  |  SPN  |  1.964  |  DISEASES
6696  |  SPP1  |  2.779  |  DISEASES
6709  |  SPTAN1  |  3.171  |  DISEASES
6714  |  SRC  |  1.675  |  DISEASES
6430  |  SRSF5  |  2.178  |  DISEASES
10274  |  STAG1  |  1.452  |  DISEASES
6772  |  STAT1  |  3.598  |  DISEASES
6775  |  STAT4  |  4.931  |  DISEASES
6776  |  STAT5A  |  1.509  |  DISEASES
29966  |  STRN3  |  1.029  |  DISEASES
6818  |  SULT1A3  |  2.977  |  DISEASES
445329  |  SULT1A4  |  3.002  |  DISEASES
6850  |  SYK  |  3.679  |  DISEASES
11346  |  SYNPO  |  1.39  |  DISEASES
80222  |  TARS2  |  1.979  |  DISEASES
123283  |  TARSL2  |  2.016  |  DISEASES
29110  |  TBK1  |  1.543  |  DISEASES
6932  |  TCF7  |  2.251  |  DISEASES
54790  |  TET2  |  1.24  |  DISEASES
200424  |  TET3  |  1.265  |  DISEASES
7018  |  TF  |  1.81  |  DISEASES
7037  |  TFRC  |  2.076  |  DISEASES
7042  |  TGFB2  |  1.188  |  DISEASES
7052  |  TGM2  |  1.306  |  DISEASES
7056  |  THBD  |  3.707  |  DISEASES
102659353  |  THRIL  |  1.017  |  DISEASES
7072  |  TIA1  |  1.57  |  DISEASES
201633  |  TIGIT  |  1.749  |  DISEASES
114609  |  TIRAP  |  1.029  |  DISEASES
7099  |  TLR4  |  3.481  |  DISEASES
7100  |  TLR5  |  4.932  |  DISEASES
51284  |  TLR7  |  5.752  |  DISEASES
54106  |  TLR9  |  5.616  |  DISEASES
340061  |  TMEM173  |  2.488  |  DISEASES
8269  |  TMEM187  |  2.425  |  DISEASES
55254  |  TMEM39A  |  3.15  |  DISEASES
7124  |  TNF  |  5.599  |  DISEASES
51330  |  TNFRSF12A  |  3.082  |  DISEASES
8784  |  TNFRSF18  |  2.67  |  DISEASES
7133  |  TNFRSF1B  |  4.229  |  DISEASES
8718  |  TNFRSF25  |  5.11  |  DISEASES
7293  |  TNFRSF4  |  2.68  |  DISEASES
8771  |  TNFRSF6B  |  1.561  |  DISEASES
3604  |  TNFRSF9  |  2.133  |  DISEASES
8742  |  TNFSF12  |  3.85  |  DISEASES
8741  |  TNFSF13  |  2.047  |  DISEASES
10673  |  TNFSF13B  |  6.438  |  DISEASES
79155  |  TNIP2  |  1.397  |  DISEASES
27327  |  TNRC6A  |  2.087  |  DISEASES
7148  |  TNXB  |  1.857  |  DISEASES
7150  |  TOP1  |  3.302  |  DISEASES
1861  |  TOR1A  |  2.52  |  DISEASES
7158  |  TP53BP1  |  1.381  |  DISEASES
8717  |  TRADD  |  1.24  |  DISEASES
7185  |  TRAF1  |  2.534  |  DISEASES
10758  |  TRAF3IP2  |  1.724  |  DISEASES
7189  |  TRAF6  |  2.308  |  DISEASES
285852  |  TREML4  |  1.315  |  DISEASES
11277  |  TREX1  |  4.927  |  DISEASES
51499  |  TRIAP1  |  6.07  |  DISEASES
10346  |  TRIM22  |  1.156  |  DISEASES
57093  |  TRIM49  |  2.08  |  DISEASES
85363  |  TRIM5  |  1.075  |  DISEASES
140691  |  TRIM69  |  1.112  |  DISEASES
6738  |  TROVE2  |  5.715  |  DISEASES
64061  |  TSPYL2  |  1.089  |  DISEASES
100287898  |  TTC34  |  1.374  |  DISEASES
7332  |  UBE2L3  |  3.1  |  DISEASES
130507  |  UBR3  |  1.157  |  DISEASES
373856  |  USP41  |  2.026  |  DISEASES
10090  |  UST  |  1.569  |  DISEASES
7409  |  VAV1  |  1.851  |  DISEASES
7421  |  VDR  |  3.064  |  DISEASES
7422  |  VEGFA  |  1.989  |  DISEASES
7441  |  VPREB1  |  1.059  |  DISEASES
57705  |  WDFY4  |  3.618  |  DISEASES
23038  |  WDTC1  |  1.66  |  DISEASES
147179  |  WIPF2  |  1.557  |  DISEASES
286046  |  XKR6  |  2.542  |  DISEASES
7520  |  XRCC5  |  1.648  |  DISEASES
2547  |  XRCC6  |  1.764  |  DISEASES
25844  |  YIPF3  |  1.114  |  DISEASES
57621  |  ZBTB2  |  1.064  |  DISEASES
79842  |  ZBTB3  |  1.33  |  DISEASES
124626  |  ZPBP2  |  1.329  |  DISEASES
Locus(Waiting for update.)
Disease ID 804
Disease lupus erythematosus
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:262)
HP:0000123  |  Nephritis  |  33
HP:0002621  |  Atherosclerosis  |  30
HP:0002633  |  Vasculitis  |  18
HP:0003613  |  Antiphospholipid antibodies  |  17
HP:0001873  |  Low platelet count  |  16
HP:0000822  |  Hypertension  |  11
HP:0001369  |  Arthritis  |  11
HP:0002960  |  Autoimmune condition  |  11
HP:0000099  |  Glomerular nephritis  |  10
HP:0000979  |  Purpura  |  10
HP:0002617  |  Aneurysmal dilatation  |  10
HP:0001903  |  Anemia  |  10
HP:0012378  |  Fatigue  |  10
HP:0010885  |  Aseptic necrosis  |  9
HP:0000709  |  Psychosis  |  9
HP:0001297  |  Cerebral vascular events  |  8
HP:0000716  |  Depression  |  8
HP:0001658  |  Myocardial infarction  |  6
HP:0003473  |  Fatigable weakness  |  6
HP:0000855  |  Insulin resistance  |  6
HP:0100614  |  Muscle inflammation  |  6
HP:0002092  |  Pulmonary artery hypertension  |  6
HP:0000112  |  Nephropathy  |  6
HP:0001298  |  Encephalopathy  |  5
HP:0002665  |  Lymphoma  |  5
HP:0002721  |  Immunodeficiency  |  5
HP:0002315  |  Headaches  |  5
HP:0003761  |  Calcinosis  |  5
HP:0000992  |  Skin photosensitivity  |  5
HP:0000488  |  Noninflammatory retina disease  |  4
HP:0001915  |  Aplastic anemia  |  4
HP:0000739  |  Anxiety  |  4
HP:0002090  |  Pneumonia  |  4
HP:0002860  |  Squamous cell carcinoma  |  4
HP:0001875  |  Neutropenia  |  4
HP:0001733  |  Pancreatic inflammation  |  4
HP:0012531  |  Pain  |  4
HP:0004389  |  Intestinal pseudo-obstruction  |  4
HP:0002664  |  Neoplasia  |  4
HP:0000708  |  Behavioral problems  |  4
HP:0002725  |  Systemic lupus erythematosus  |  4
HP:0001370  |  Rheumatoid arthritis  |  4
HP:0100512  |  Vitamin D deficiency  |  3
HP:0002027  |  Abdominal pain  |  3
HP:0100543  |  Cognitive deficits  |  3
HP:0004416  |  Precocious atherosclerosis  |  3
HP:0012115  |  Liver inflammation  |  3
HP:0000752  |  Hyperactive behavior  |  3
HP:0004942  |  Aortic aneurysm  |  3
HP:0000969  |  Dropsy  |  3
HP:0100280  |  Morbus Crohn  |  3
HP:0100658  |  Bacterial infection of skin  |  3
HP:0001888  |  Lymphocytopenia  |  3
HP:0002352  |  Leukoencephalopathy  |  3
HP:0009830  |  Peripheral neuritis  |  3
HP:0002102  |  Pleuritis  |  3
HP:0000820  |  Thyroid abnormality  |  3
HP:0002243  |  Protein-losing enteropathy  |  3
HP:0000083  |  Renal insufficiency  |  3
HP:0011974  |  Myelofibrosis  |  3
HP:0030731  |  Carcinoma  |  3
HP:0002202  |  Pleural effusion  |  3
HP:0002242  |  Enteropathy  |  3
HP:0030880  |  Raynaud phenomenon  |  3
HP:0001677  |  Coronary artery disease  |  3
HP:0001735  |  Acute pancreatitis  |  3
HP:0100550  |  Rupture of tendons  |  3
HP:0000819  |  Diabetes mellitus  |  3
HP:0000572  |  Visual loss  |  3
HP:0006510  |  Chronic obstructive pulmonary disease  |  2
HP:0004944  |  Cerebral artery aneurysm  |  2
HP:0100522  |  Thymoma  |  2
HP:0001701  |  Pericarditis  |  2
HP:0100699  |  Scarring  |  2
HP:0002459  |  Dysautonomia  |  2
HP:0001878  |  Haemolytic anaemia  |  2
HP:0006775  |  Multiple myeloma  |  2
HP:0002140  |  Ischemic stroke  |  2
HP:0002099  |  Asthma  |  2
HP:0001287  |  Meningitis  |  2
HP:0004431  |  Complement deficiency  |  2
HP:0012622  |  Chronic kidney disease  |  2
HP:0001659  |  Aortic insufficiency  |  2
HP:0001907  |  Thromboembolic disease  |  2
HP:0100324  |  Progressive systemic scleroderma  |  2
HP:0003765  |  Psoriasis  |  2
HP:0002354  |  Memory loss  |  2
HP:0000100  |  Nephrosis  |  2
HP:0006530  |  Interstitial lung disease  |  2
HP:0004859  |  Amegakaryocytic thrombocytopenia  |  2
HP:0010702  |  Hypergammaglobulinaemia  |  2
HP:0000821  |  Underactive thyroid  |  2
HP:0002076  |  Migraine headaches  |  2
HP:0004950  |  Peripheral artery disease  |  2
HP:0012490  |  Inflammation of fat tissue  |  2
HP:0100665  |  Angiooedema  |  2
HP:0001945  |  Fever  |  2
HP:0007417  |  Discoid lupus erythematosus  |  2
HP:0002583  |  Colitis  |  2
HP:0000490  |  Sunken eyes  |  2
HP:0002863  |  Myelodysplastic syndrome  |  2
HP:0001250  |  Seizures  |  2
HP:0003774  |  End-stage renal failure  |  2
HP:0045073  |  Serositis  |  2
HP:0012410  |  Pure red cell aplasia  |  2
HP:0002720  |  Decreased immunoglobulin A  |  2
HP:0005523  |  Lymphoproliferative disorder  |  2
HP:0100806  |  Sepsis  |  2
HP:0002516  |  Intracranial pressure elevation  |  2
HP:0012486  |  Inflammation of spinal cord  |  2
HP:0002107  |  Collapsed lung  |  2
HP:0001635  |  Congestive heart failure  |  1
HP:0000141  |  Abnormal absence of menstruation  |  1
HP:0012579  |  Minimal change glomerulonephritis  |  1
HP:0007302  |  Bipolar disorder  |  1
HP:0002500  |  Leukoaraiosis  |  1
HP:0002910  |  Elevated transaminases  |  1
HP:0011675  |  Arrhythmias  |  1
HP:0006859  |  Posterior leukoencephalopathy  |  1
HP:0100539  |  Periorbital swelling  |  1
HP:0000096  |  Glomerulosclerosis  |  1
HP:0001061  |  Acne  |  1
HP:0100718  |  Uterine rupture  |  1
HP:0100653  |  Optic neuritis  |  1
HP:0000956  |  Keratosis nigricans  |  1
HP:0002605  |  Hepatic necrosis  |  1
HP:0012344  |  Morphea  |  1
HP:0001289  |  Confusion  |  1
HP:0003095  |  Septic arthritis  |  1
HP:0002890  |  Thyroid carcinoma  |  1
HP:0001909  |  Leukemia  |  1
HP:0012588  |  Steroid-resistant nephrotic syndrome  |  1
HP:0012223  |  Ruptured spleen  |  1
HP:0005305  |  Cerebral vein thrombosis  |  1
HP:0100532  |  Scleritis  |  1
HP:0001410  |  Decreased liver function  |  1
HP:0007380  |  Facial telangiectatic vessels  |  1
HP:0000790  |  Hematuria  |  1
HP:0002514  |  Intracranial calcifications  |  1
HP:0012722  |  Heart block  |  1
HP:0001890  |  Autoimmune hemolytic anemia  |  1
HP:0012075  |  Personality disorder  |  1
HP:0000501  |  Glaucoma  |  1
HP:0002232  |  Patchy alopecia  |  1
HP:0012133  |  Erythroid hypoplasia  |  1
HP:0000963  |  Thin skin  |  1
HP:0200029  |  Cutaneous vasculitis  |  1
HP:0007018  |  Attention deficits  |  1
HP:0011695  |  Cerebellar hemorrhage  |  1
HP:0001663  |  Ventricular fibrillation  |  1
HP:0000843  |  Hyperparathyroidism  |  1
HP:0010280  |  Stomatitis  |  1
HP:0001581  |  Recurrent skin infections  |  1
HP:0011450  |  CNS infection  |  1
HP:0002206  |  Pulmonary fibrosis  |  1
HP:0000939  |  Osteoporosis  |  1
HP:0001279  |  Syncope  |  1
HP:0002093  |  progressive respiratory failure  |  1
HP:0001045  |  Blotchy loss of skin color  |  1
HP:0000938  |  Decreased bone mineral density  |  1
HP:0012641  |  Decreased intracranial pressure  |  1
HP:0002138  |  Subarachnoid hemorrhage  |  1
HP:0002729  |  Follicular hyperplasia  |  1
HP:0002204  |  Pulmonary embolism  |  1
HP:0001919  |  Acute renal failure  |  1
HP:0011096  |  Demyelination  |  1
HP:0002133  |  Status epilepticus  |  1
HP:0011900  |  Hypofibrinogenemia  |  1
HP:0001943  |  Hypoglycemia  |  1
HP:0002273  |  Tetraparesis  |  1
HP:0012156  |  Hemophagocytosis  |  1
HP:0030065  |  Primitive neuroectodermal tumor  |  1
HP:0000651  |  Diplopia  |  1
HP:0002829  |  Arthralgias  |  1
HP:0002634  |  Arteriosclerosis  |  1
HP:0012126  |  Gastric cancer  |  1
HP:0100607  |  Painful menstruation  |  1
HP:0001596  |  Hair loss  |  1
HP:0001025  |  Hives  |  1
HP:0000121  |  Nephrocalcinosis  |  1
HP:0005942  |  Desquamative interstitial pneumonitis  |  1
HP:0003073  |  Hypoalbuminaemia  |  1
HP:0200043  |  Verrucae  |  1
HP:0000789  |  Infertility  |  1
HP:0004395  |  Malnutrition  |  1
HP:0100033  |  Tic disorder  |  1
HP:0002922  |  Increased CSF protein  |  1
HP:0200034  |  Papule  |  1
HP:0001947  |  Renal tubular acidosis  |  1
HP:0001928  |  Abnormal blood coagulation studies  |  1
HP:0002383  |  Encephalitis  |  1
HP:0100758  |  Gangrene  |  1
HP:0100633  |  Inflammation of the esophagus  |  1
HP:0030692  |  Brain tumor  |  1
HP:0002895  |  Papillary thyroid carcinoma  |  1
HP:0007544  |  Piebaldism  |  1
HP:0001751  |  Vestibular dysfunction  |  1
HP:0000867  |  Secondary hyperparathyroidism  |  1
HP:0001638  |  Cardiomyopathy  |  1
HP:0001251  |  Ataxia  |  1
HP:0000704  |  Pyorrhea  |  1
HP:0011944  |  Small vessel vasculitis  |  1
HP:0003470  |  Inability to move  |  1
HP:0012281  |  Chylous ascites  |  1
HP:0002907  |  Microhematuria  |  1
HP:0000407  |  sensorineural hearing loss  |  1
HP:0003201  |  Rhabdomyolysis  |  1
HP:0003198  |  Myopathic changes  |  1
HP:0000823  |  Pubertal delay  |  1
HP:0012578  |  Membranous glomerulonephritis  |  1
HP:0001541  |  Ascites  |  1
HP:0012727  |  Thoracic aortic aneurysm  |  1
HP:0100825  |  Inflammation of the lips  |  1
HP:0004326  |  Cachexia  |  1
HP:0100646  |  Thyroiditis  |  1
HP:0100584  |  Endocarditis  |  1
HP:0012740  |  Papilloma  |  1
HP:0000126  |  Hydronephrosis  |  1
HP:0001698  |  Pericardial effusions  |  1
HP:0002647  |  Aortic dissection  |  1
HP:0030350  |  Erythematous papule  |  1
HP:0003040  |  Arthropathy  |  1
HP:0002840  |  Lymphadenitis  |  1
HP:0001324  |  Muscular weakness  |  1
HP:0001047  |  Atopic dermatitis  |  1
HP:0004943  |  Accelerated atherosclerosis  |  1
HP:0010302  |  Tumor of the spinal cord  |  1
HP:0001300  |  Parkinsonism  |  1
HP:0004818  |  Paroxysmal nocturnal hemoglobinuria  |  1
HP:0001394  |  Hepatic cirrhosis  |  1
HP:0030882  |  Enlargement of the diameter (cross-section) of a coronary artery.  |  1
HP:0100310  |  Extradural hematoma  |  1
HP:0030069  |  Primary central nervous system lymphoma  |  1
HP:0012089  |  Arteritis  |  1
HP:0001973  |  Autoimmune thrombocytopenia  |  1
HP:0000656  |  Ectropion  |  1
HP:0003002  |  Breast carcinoma  |  1
HP:0000872  |  Hashimoto's thyroiditis  |  1
HP:0000829  |  Hypoparathyroidism  |  1
HP:0003641  |  Hemoglobin in urine  |  1
HP:0002615  |  Low blood pressure  |  1
HP:0006689  |  Bacterial endocarditis  |  1
HP:0002072  |  Chorea  |  1
HP:0012636  |  Retinal vein occlusion  |  1
HP:0002196  |  Myelopathy  |  1
HP:0006824  |  Cranial nerve palsy  |  1
HP:0030127  |  Endometriosis  |  1
HP:0003493  |  Elevated antinuclear antibody  |  1
HP:0002170  |  Intracranial hemorrhage  |  1
HP:0000097  |  focal glomerulosclerosis  |  1
HP:0004929  |  Coronary artherosclerosis  |  1
HP:0000093  |  Proteinuria  |  1
HP:0012191  |  B-cell lymphoma  |  1
HP:0002716  |  Lymph node hyperplasia  |  1
HP:0010566  |  Hamartoma  |  1
HP:0006515  |  Interstitial pneumonitis  |  1
HP:0005206  |  Pancreatic pseudocyst  |  1
HP:0100754  |  Mania  |  1
HP:0100578  |  Lipoatrophy  |  1
HP:0004936  |  Blood clot in vein  |  1
HP:0001622  |  Premature delivery  |  1
HP:0012190  |  T cell lymphoma  |  1
Disease ID 804
Disease lupus erythematosus
Manually Symptom
UMLS  | Name(Total Manually Symptoms:79)
C2364133  |  infection
C2364072  |  depression
C2186740  |  urticaria
C2046121  |  aortic dissection
C1963220  |  pulmonary hypertension
C1963211  |  pericarditis
C1963138  |  hypertension
C1962971  |  myocarditis
C1868885  |  uncontrolled hypertension
C1705714  |  warts
C1403411  |  lymphadenosis cutis benigna
C1402315  |  vascular lesions
C1253937  |  pericardial effusion
C1000483  |  anemia
C0857305  |  thrombocytopenic purpura
C0743711  |  eye lesion
C0742115  |  cerebritis
C0393799  |  miller-fisher syndrome
C0376293  |  stigmata
C0272242  |  complement deficiency
C0265145  |  chronic pericarditis with effusion
C0263390  |  papular mucinosis
C0263367  |  koebner phenomenon
C0262988  |  cutaneous vasculitis
C0242666  |  protein s deficiency
C0234962  |  pulmonary vasculitis
C0234906  |  annular erythema
C0233401  |  psychiatric symptom
C0221011  |  malignant atrophic papulosis
C0162855  |  mucinosis
C0155773  |  portal vein thrombosis
C0151205  |  periorbital edema
C0085932  |  bullous skin disease
C0085636  |  light sensitivity
C0042900  |  vitiligo
C0042373  |  vascular disorders
C0041327  |  pulmonary tuberculosis
C0040053  |  thrombosis
C0040034  |  thrombocytopenia
C0037285  |  skin manifestations
C0037284  |  skin lesions
C0037284  |  skin lesion
C0037274  |  skin disease
C0033975  |  psychosis
C0033774  |  pruritus
C0032453  |  relapsing polychondritis
C0031736  |  polymorphous light eruption
C0031048  |  constrictive pericarditis
C0030326  |  panniculitis
C0029166  |  oral manifestations
C0029118  |  opportunistic infection
C0027726  |  nephrotic syndrome
C0027697  |  nephritis
C0027051  |  myocardial infarction
C0026848  |  myopathy
C0024312  |  lymphocytopenia
C0023223  |  leg ulcers
C0022658  |  renal disease
C0022658  |  nephropathy
C0022408  |  arthropathy
C0019829  |  malignant lymphogranulomatosis
C0019080  |  hemorrhage
C0018784  |  sensorineural hearing loss
C0017658  |  glomerulonephritis
C0017181  |  gastrointestinal hemorrhage
C0017086  |  gangrene
C0016436  |  folliculitides
C0016085  |  filariasis
C0016053  |  fibromyalgia
C0015458  |  progressive hemifacial atrophy
C0015230  |  rash
C0013182  |  drug hypersensitivity
C0012739  |  disseminated intravascular coagulation
C0007114  |  cancer of the skin
C0006840  |  moniliasis
C0005779  |  coagulation disorder
C0004610  |  bacteremia
C0002880  |  autoimmune hemolytic anemia
C0002171  |  alopecia areata
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:42)
C0009450  |  infection  |  34
C0027697  |  nephritis  |  33
C0040034  |  thrombocytopenia  |  16
C0020538  |  hypertension  |  11
C0019080  |  hemorrhage  |  11
C0022658  |  renal disease  |  11
C0017658  |  glomerulonephritis  |  10
C0033975  |  psychosis  |  9
C0040053  |  thrombosis  |  9
C0034153  |  thrombocytopenic purpura  |  9
C0011570  |  depression  |  8
C0002871  |  anemia  |  6
C0022658  |  nephropathy  |  6
C0233401  |  psychiatric symptom  |  6
C0027051  |  myocardial infarction  |  6
C0020542  |  pulmonary hypertension  |  6
C0162855  |  mucinosis  |  5
C0037284  |  skin lesion  |  5
C0037284  |  skin lesions  |  4
C0015230  |  rash  |  3
C0037285  |  skin manifestations  |  2
C0030326  |  panniculitis  |  2
C0027726  |  nephrotic syndrome  |  2
C0272242  |  complement deficiency  |  2
C0031046  |  pericarditis  |  2
C0262988  |  cutaneous vasculitis  |  1
C0263367  |  koebner phenomenon  |  1
C0017086  |  gangrene  |  1
C0031039  |  pericardial effusion  |  1
C0002880  |  autoimmune hemolytic anemia  |  1
C1402315  |  vascular lesions  |  1
C0018784  |  sensorineural hearing loss  |  1
C0042109  |  urticaria  |  1
C0042900  |  vitiligo  |  1
C0042373  |  vascular disorders  |  1
C0022408  |  arthropathy  |  1
C0004610  |  bacteremia  |  1
C0151205  |  periorbital edema  |  1
C0026848  |  myopathy  |  1
C0043037  |  warts  |  1
C0340643  |  aortic dissection  |  1
C0029166  |  oral manifestations  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
Text Mining Genotype(Total Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:21)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs105164872190095155024BANK1umls:C0409974BeFreeThe dual effect of the lupus-associated polymorphism rs10516487 on BANK1 gene expression and protein localization.0.0005428842012BANK14101829919GT,A
rs1143679225861643684ITGAMumls:C0409974BeFreeThe rs1143679 (R77H) lupus associated variant of ITGAM (CD11b) impairs complement receptor 3 mediated functions in human monocytes.0.0021715352012ITGAM1631265490GA
rs1143679246082263684ITGAMumls:C0409974BeFreeCombined protein- and nucleic acid-level effects of rs1143679 (R77H), a lupus-predisposing variant within ITGAM.0.0021715352015ITGAM1631265490GA
rs1270942219529183663IRF5umls:C0409974BeFreeImportantly, our data suggest that in patients with lupus, the presence of the HLA lupus risk alleles in rs1270942 and rs3131379 increases the odds of also carrying the lupus risk allele in IRF5 (rs2070197) by 17% and 16%, respectively (P = 0.0028 and P = 0.0047, respectively).0.018273822012CFB631951083AG
rs13023380234411362547XRCC6umls:C0409974BeFreeDNA carrying the intronic risk allele rs13023380 showed reduced binding efficiency to a cellular protein complex including nucleolin and lupus autoantigen Ku70/80, and showed reduced transcriptional activity in vivo.0.0005428842013IFIH12162297853GA
rs13023380234411364691NCLumls:C0409974BeFreeDNA carrying the intronic risk allele rs13023380 showed reduced binding efficiency to a cellular protein complex including nucleolin and lupus autoantigen Ku70/80, and showed reduced transcriptional activity in vivo.0.0002714422013IFIH12162297853GA
rs2070197219529183663IRF5umls:C0409974BeFreeImportantly, our data suggest that in patients with lupus, the presence of the HLA lupus risk alleles in rs1270942 and rs3131379 increases the odds of also carrying the lupus risk allele in IRF5 (rs2070197) by 17% and 16%, respectively (P = 0.0028 and P = 0.0047, respectively).0.018273822012IRF57128948946TC
rs24766012335956226191PTPN22umls:C0409974BeFreeThe protein tyrosine phosphatase LYP, a key regulator of TCR signaling, presents a single nucleotide polymorphism, C1858T, associated with several autoimmune diseases such as type I diabetes, rheumatoid arthritis, and lupus.0.0268516772013PTPN22;AP4B1-AS11113834946AG
rs24766011875929526191PTPN22umls:C0409974BeFreeThe PTPN22 C1858T polymorphism is associated with skewing of cytokine profiles toward high interferon-alpha activity and low tumor necrosis factor alpha levels in patients with lupus.0.0268516772008PTPN22;AP4B1-AS11113834946AG
rs24766011605256326191PTPN22umls:C0409974GAD[ The R620W polymorphism of the PTPN22 gene is not a major risk allele for SLE susceptibility in our sample of Caucasian individuals from northern America, the UK, or Finland, but it appears to be a risk factor for the concurrent autoimmune diseases of aut]0.0268516772005PTPN22;AP4B1-AS11113834946AG
rs24766011527393426191PTPN22umls:C0409974GAD[Together with recent evidence showing association of this SNP with type 1 diabetes and rheumatoid arthritis, these data provide compelling evidence that PTPN22 plays a fundamental role in regulating the immune system and the development of autoimmunity.]0.0268516772004PTPN22;AP4B1-AS11113834946AG
rs2476601187592957124TNFumls:C0409974BeFreeThe PTPN22 C1858T polymorphism is associated with skewing of cytokine profiles toward high interferon-alpha activity and low tumor necrosis factor alpha levels in patients with lupus.0.020369412008PTPN22;AP4B1-AS11113834946AG
rs24766012335956252ACP1umls:C0409974BeFreeThe protein tyrosine phosphatase LYP, a key regulator of TCR signaling, presents a single nucleotide polymorphism, C1858T, associated with several autoimmune diseases such as type I diabetes, rheumatoid arthritis, and lupus.0.0002714422013PTPN22;AP4B1-AS11113834946AG
rs24766011575901226191PTPN22umls:C0409974GAD[Altogether, we have provided further evidence of an association between autoimmune diseases and the 1858C>T polymorphism in PTPN22.]0.0268516772005PTPN22;AP4B1-AS11113834946AG
rs3131379219529183663IRF5umls:C0409974BeFreeImportantly, our data suggest that in patients with lupus, the presence of the HLA lupus risk alleles in rs1270942 and rs3131379 increases the odds of also carrying the lupus risk allele in IRF5 (rs2070197) by 17% and 16%, respectively (P = 0.0028 and P = 0.0047, respectively).0.018273822012MSH5;MSH5-SAPCD1631753256GA
rs3813946173604601380CR2umls:C0409974BeFreeSingle-nucleotide polymorphism 1 (rs3813946), located in the 5' untranslated region of the CR2 gene, altered transcriptional activity, suggesting a potential mechanism by which CR2 could contribute to the development of lupus.0.0031813582007CR21207454348TC
rs4649203240708584792NFKBIAumls:C0409974BeFreeWe found that these two SNPs (rs8016947 and rs4649203) in two loci (NFKBIA and IL28RA) were associated with psoriasis and SLE with genome-wide significance (Pcombined<5×10(-8) in psoriasis and Pcombined<5×10(-8) in SLE): rs8016947 at NFKBIA (Pcombined-psoriasis=3.90×10(-10), Pcombined-SLE=1.08×10(-13)) and rs4649203 at IL28RA (Pcombined-psoriasis=3.91×10(-12), Pcombined-SLE=9.90×10(-9)).0.0002714422014NA124193430GA
rs464920324070858163702IFNLR1umls:C0409974BeFreeWe found that these two SNPs (rs8016947 and rs4649203) in two loci (NFKBIA and IL28RA) were associated with psoriasis and SLE with genome-wide significance (Pcombined<5×10(-8) in psoriasis and Pcombined<5×10(-8) in SLE): rs8016947 at NFKBIA (Pcombined-psoriasis=3.90×10(-10), Pcombined-SLE=1.08×10(-13)) and rs4649203 at IL28RA (Pcombined-psoriasis=3.91×10(-12), Pcombined-SLE=9.90×10(-9)).0.0002714422014NA124193430GA
rs725565542193742411277TREX1umls:C0409974BeFreeThe TREX1 exonuclease R114H mutation in Aicardi-Goutières syndrome and lupus reveals dimeric structure requirements for DNA degradation activity.0.0019000932011TREX1348466996GA,C
rs8016947240708584792NFKBIAumls:C0409974BeFreeWe found that these two SNPs (rs8016947 and rs4649203) in two loci (NFKBIA and IL28RA) were associated with psoriasis and SLE with genome-wide significance (Pcombined<5×10(-8) in psoriasis and Pcombined<5×10(-8) in SLE): rs8016947 at NFKBIA (Pcombined-psoriasis=3.90×10(-10), Pcombined-SLE=1.08×10(-13)) and rs4649203 at IL28RA (Pcombined-psoriasis=3.91×10(-12), Pcombined-SLE=9.90×10(-9)).0.0002714422014NA1435363460TG
rs801694724070858163702IFNLR1umls:C0409974BeFreeWe found that these two SNPs (rs8016947 and rs4649203) in two loci (NFKBIA and IL28RA) were associated with psoriasis and SLE with genome-wide significance (Pcombined<5×10(-8) in psoriasis and Pcombined<5×10(-8) in SLE): rs8016947 at NFKBIA (Pcombined-psoriasis=3.90×10(-10), Pcombined-SLE=1.08×10(-13)) and rs4649203 at IL28RA (Pcombined-psoriasis=3.91×10(-12), Pcombined-SLE=9.90×10(-9)).0.0002714422014NA1435363460TG
GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)
GWASdb Snp Trait(Total Genotypes:5)
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
1195531423rs1890645TCrs1890645206620654.00E-06NA2.98[1.88-4.73] 116 European American ancestry cases; 3,351 European American ancestry controlsEuropean American(3467)ALL(3467)EUR(3467)ALL(3467)Neonatal lupusHPOID:0002960AutoimmunityDOID:8857lupus erythematosusD008180Lupus Erythematosus, SystemicEFOID:0004537neonatal systemic lupus erthematosusLupus erythematosusNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tResearch Support, U.S. Gov't, Non-P.H.S.
631448976rs3099844CArs3099844206620655.00E-10NA3.34[2.29-4.89]116 European American ancestry cases; 3,351 European American ancestry controlsEuropean American(3467)ALL(3467)EUR(3467)ALL(3467)Neonatal lupusHPOID:0002960AutoimmunityDOID:8857lupus erythematosusD008180Lupus Erythematosus, SystemicEFOID:0004537neonatal systemic lupus erthematosusLupus erythematosusNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tResearch Support, U.S. Gov't, Non-P.H.S.
104719796rs1391511AGrs1391511206620657.00E-06NA1.84[1.41-2.40] 116 European American ancestry cases; 3,351 European American ancestry controlsEuropean American(3467)ALL(3467)EUR(3467)ALL(3467)Neonatal lupusHPOID:0002960AutoimmunityDOID:8857lupus erythematosusD008180Lupus Erythematosus, SystemicEFOID:0004537neonatal systemic lupus erthematosusLupus erythematosusNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tResearch Support, U.S. Gov't, Non-P.H.S.
1284008275rs2403106AGrs2403106206620653.00E-06NA2.48[1.70-3.61] 116 European American ancestry cases; 3,351 European American ancestry controlsEuropean American(3467)ALL(3467)EUR(3467)ALL(3467)Neonatal lupusHPOID:0002960AutoimmunityDOID:8857lupus erythematosusD008180Lupus Erythematosus, SystemicEFOID:0004537neonatal systemic lupus erthematosusLupus erythematosusNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tResearch Support, U.S. Gov't, Non-P.H.S.
2140056423rs743446ACrs743446206620655.00E-06NA2.4[1.64-3.49] 116 European American ancestry cases; 3,351 European American ancestry controlsEuropean American(3467)ALL(3467)EUR(3467)ALL(3467)Neonatal lupusHPOID:0002960AutoimmunityDOID:8857lupus erythematosusD008180Lupus Erythematosus, SystemicEFOID:0004537neonatal systemic lupus erthematosusLupus erythematosusNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tResearch Support, U.S. Gov't, Non-P.H.S.
Mapped by lexical matching(Total Items:0)
(Waiting for update.)
Mapped by homologous gene(Total Items:0)
(Waiting for update.)
Disease ID 804
Disease lupus erythematosus
Case(Waiting for update.)