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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine



   aspergillosis
  

Disease ID 928
Disease aspergillosis
Definition
Infections with fungi of the genus ASPERGILLUS.
Synonym
[x]aspergillosis, unspecified
[x]aspergillosis, unspecified (disorder)
aspergillose
aspergilloses
aspergillosis (disorder)
aspergillosis [disease/finding]
aspergillosis, nos
infection due to aspergillus
Orphanet
DOID
UMLS
C0004030
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:94)
C0010674  |  cystic fibrosis  |  17
C0004096  |  asthma  |  13
C0024117  |  chronic obstructive pulmonary disease  |  10
C0024115  |  pulmonary disease  |  10
C0600260  |  obstructive pulmonary disease  |  10
C0376545  |  hematological malignancies  |  9
C0023418  |  leukemia  |  8
C0242379  |  lung cancer  |  7
C0376545  |  hematologic malignancies  |  7
C0018203  |  chronic granulomatous disease  |  5
C0027947  |  neutropenia  |  5
C0409974  |  lupus erythematosus  |  4
C0023470  |  myeloid leukaemia  |  4
C0024141  |  systemic lupus erythematosus  |  4
C0023467  |  acute myeloid leukaemia  |  4
C0032285  |  pneumonia  |  4
C0021400  |  influenza  |  4
C0085669  |  acute leukemia  |  3
C0376545  |  hematologic malignancy  |  3
C0036202  |  sarcoidosis  |  2
C0023470  |  myelogenous leukemia  |  2
C0011847  |  diabetes  |  2
C0006267  |  bronchiectasis  |  2
C0026946  |  fungal infection  |  2
C0023470  |  myeloid leukemia  |  2
C0023448  |  lymphocytic leukemia  |  2
C0041296  |  tuberculosis  |  2
C0004623  |  bacterial infection  |  2
C0023467  |  acute myeloid leukemia  |  2
C0023467  |  acute myelogenous leukemia  |  2
C0009324  |  ulcerative colitis  |  2
C0026718  |  mucormycosis  |  2
C0023418  |  leukaemia  |  2
C0019158  |  hepatitis  |  1
C0024110  |  lung abscess  |  1
C0002871  |  anemia  |  1
C0003873  |  rheumatoid arthritis  |  1
C0008370  |  cholestasis  |  1
C0013502  |  hydatid disease  |  1
C0684249  |  carcinoma of lung  |  1
C0022398  |  hyper-ige syndrome  |  1
C0024115  |  pulmonary diseases  |  1
C0009319  |  colitis  |  1
C0023895  |  liver disease  |  1
C0242770  |  cryptogenic organizing pneumonia  |  1
C0023890  |  cirrhosis  |  1
C0023449  |  acute lymphoblastic leukemia  |  1
C0684249  |  lung carcinoma  |  1
C0004096  |  bronchial asthma  |  1
C0026470  |  monoclonal gammopathy of undetermined significance  |  1
C0019621  |  langerhans cell histiocytosis  |  1
C0023343  |  leprosy  |  1
C0376545  |  hematological malignancy  |  1
C0023449  |  acute lymphocytic leukemia  |  1
C0024530  |  malaria  |  1
C0038218  |  acute severe asthma  |  1
C1527311  |  brain swelling  |  1
C0034069  |  pulmonary fibrosis  |  1
C0024299  |  lymphoma  |  1
C0019187  |  alcoholic hepatitis  |  1
C0012739  |  disseminated intravascular coagulation  |  1
C0037199  |  sinusitis  |  1
C0007134  |  renal cell carcinoma  |  1
C0004623  |  bacterial infections  |  1
C0026975  |  myelitis  |  1
C0002874  |  aplastic anemia  |  1
C0035204  |  respiratory disease  |  1
C0034072  |  pulmonary heart disease  |  1
C0006840  |  candidiasis  |  1
C0023434  |  chronic lymphocytic leukemia  |  1
C0041956  |  ureteral obstruction  |  1
C0023890  |  liver cirrhosis  |  1
C0024117  |  chronic obstructive pulmonary disease (copd)  |  1
C0024305  |  non-hodgkin lymphoma  |  1
C0003864  |  arthritis  |  1
C0035204  |  respiratory diseases  |  1
C0001261  |  actinomycosis  |  1
C0600260  |  obstructive pulmonary diseases  |  1
C0018799  |  heart disease  |  1
C0042769  |  virus infection  |  1
C0039590  |  testicular cancer  |  1
C0041327  |  pulmonary tuberculosis  |  1
C1136085  |  monoclonal gammopathy  |  1
C0019618  |  histiocytosis  |  1
C0011633  |  dermatomyositis  |  1
C0007121  |  bronchogenic carcinoma  |  1
C0026946  |  fungal infections  |  1
C0023448  |  lymphoblastic leukemia  |  1
C0178879  |  obstructive uropathy  |  1
C0042075  |  uropathy  |  1
C0023530  |  leucopenia  |  1
C0042384  |  vasculitis  |  1
C0019829  |  hodgkin lymphoma  |  1
C0948187  |  tracheomalacia  |  1
Curated Gene(Waiting for update.)
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:4)
64581  |  CLEC7A  |  CIPHER
7096  |  TLR1  |  CIPHER
7099  |  TLR4  |  CIPHER
10333  |  TLR6  |  CIPHER
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:93)
369  |  ARAF  |  2.36  |  DISEASES
11016  |  ATF7  |  3.169  |  DISEASES
801  |  CALM1  |  3.366  |  DISEASES
64170  |  CARD9  |  2.228  |  DISEASES
6364  |  CCL20  |  2.32  |  DISEASES
914  |  CD2  |  1.314  |  DISEASES
959  |  CD40LG  |  3.21  |  DISEASES
1043  |  CD52  |  2.329  |  DISEASES
974  |  CD79B  |  1.149  |  DISEASES
9308  |  CD83  |  1.516  |  DISEASES
942  |  CD86  |  1.896  |  DISEASES
4267  |  CD99  |  1.967  |  DISEASES
1118  |  CHIT1  |  1.688  |  DISEASES
93978  |  CLEC6A  |  2.837  |  DISEASES
1363  |  CPE  |  1.105  |  DISEASES
27297  |  CRCP  |  1.287  |  DISEASES
1394  |  CRHR1  |  2.917  |  DISEASES
2919  |  CXCL1  |  1.231  |  DISEASES
2920  |  CXCL2  |  2.634  |  DISEASES
1536  |  CYBB  |  1.009  |  DISEASES
1557  |  CYP2C19  |  4.044  |  DISEASES
1576  |  CYP3A4  |  2.797  |  DISEASES
10521  |  DDX17  |  1.2  |  DISEASES
51428  |  DDX41  |  1.163  |  DISEASES
163486  |  DENND1B  |  1.977  |  DISEASES
51071  |  DERA  |  1.466  |  DISEASES
5169  |  ENPP3  |  2.366  |  DISEASES
54206  |  ERRFI1  |  1.486  |  DISEASES
201456  |  FBXO15  |  2.418  |  DISEASES
2219  |  FCN1  |  2.191  |  DISEASES
2318  |  FLNC  |  8.628  |  DISEASES
53827  |  FXYD5  |  2.489  |  DISEASES
10755  |  GIPC1  |  1.023  |  DISEASES
160897  |  GPR180  |  2.886  |  DISEASES
283902  |  HCCAT5  |  1.757  |  DISEASES
55733  |  HHAT  |  5.001  |  DISEASES
3240  |  HP  |  1.18  |  DISEASES
3320  |  HSP90AA1  |  2.687  |  DISEASES
3586  |  IL10  |  3.216  |  DISEASES
3605  |  IL17A  |  2.575  |  DISEASES
149233  |  IL23R  |  1.069  |  DISEASES
246778  |  IL27  |  1.061  |  DISEASES
3684  |  ITGAM  |  1.616  |  DISEASES
3767  |  KCNJ11  |  1.312  |  DISEASES
3916  |  LAMP1  |  1.269  |  DISEASES
3920  |  LAMP2  |  1.638  |  DISEASES
7044  |  LEFTY2  |  1.104  |  DISEASES
8825  |  LIN7A  |  1.398  |  DISEASES
987  |  LRBA  |  1.788  |  DISEASES
10046  |  MAMLD1  |  1.035  |  DISEASES
4153  |  MBL2  |  2.245  |  DISEASES
196410  |  METTL7B  |  1.313  |  DISEASES
4519  |  MT-CYB  |  1.857  |  DISEASES
727897  |  MUC5B  |  1.73  |  DISEASES
4615  |  MYD88  |  2.094  |  DISEASES
4688  |  NCF2  |  2.949  |  DISEASES
84504  |  NKX6-2  |  1.878  |  DISEASES
64318  |  NOC3L  |  2.163  |  DISEASES
131870  |  NUDT16  |  1.431  |  DISEASES
5164  |  PDK2  |  1.433  |  DISEASES
5238  |  PGM3  |  1.002  |  DISEASES
5251  |  PHEX  |  1.27  |  DISEASES
5255  |  PHKA1  |  1.998  |  DISEASES
55124  |  PIWIL2  |  1.699  |  DISEASES
26279  |  PLA2G2D  |  1.077  |  DISEASES
8605  |  PLA2G4C  |  1.811  |  DISEASES
5322  |  PLA2G5  |  1.709  |  DISEASES
151056  |  PLB1  |  2.804  |  DISEASES
9701  |  PPP6R2  |  2.415  |  DISEASES
5578  |  PRKCA  |  1.868  |  DISEASES
83695  |  RHNO1  |  3.852  |  DISEASES
22928  |  SEPHS2  |  2.226  |  DISEASES
729238  |  SFTPA2  |  3.343  |  DISEASES
6441  |  SFTPD  |  2.2  |  DISEASES
59307  |  SIGIRR  |  1.055  |  DISEASES
6510  |  SLC1A5  |  1.351  |  DISEASES
23583  |  SMUG1  |  1.528  |  DISEASES
6850  |  SYK  |  1.955  |  DISEASES
5726  |  TAS2R38  |  1.048  |  DISEASES
54790  |  TET2  |  1.231  |  DISEASES
7096  |  TLR1  |  1.578  |  DISEASES
7099  |  TLR4  |  3.093  |  DISEASES
10333  |  TLR6  |  1.911  |  DISEASES
54106  |  TLR9  |  2.801  |  DISEASES
387521  |  TMEM189  |  2.962  |  DISEASES
7124  |  TNF  |  3.139  |  DISEASES
7133  |  TNFRSF1B  |  2.081  |  DISEASES
3604  |  TNFRSF9  |  1.3  |  DISEASES
1861  |  TOR1A  |  1.137  |  DISEASES
7306  |  TYRP1  |  1.495  |  DISEASES
7409  |  VAV1  |  1.188  |  DISEASES
51530  |  ZC3HC1  |  1.657  |  DISEASES
148266  |  ZNF569  |  1.146  |  DISEASES
Locus(Waiting for update.)
Disease ID 928
Disease aspergillosis
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:64)
HP:0002099  |  Asthma  |  14
HP:0006510  |  Chronic obstructive pulmonary disease  |  10
HP:0001909  |  Leukemia  |  8
HP:0002725  |  Systemic lupus erythematosus  |  4
HP:0001875  |  Neutropenia  |  4
HP:0004808  |  Acute myelogenous leukemia  |  4
HP:0001399  |  Liver failure  |  4
HP:0002664  |  Neoplasia  |  4
HP:0030731  |  Carcinoma  |  3
HP:0100632  |  Pulmonary sequestration  |  3
HP:0002105  |  Hemoptysis  |  3
HP:0002090  |  Pneumonia  |  3
HP:0012735  |  Coughing  |  3
HP:0002488  |  Acute leukemias  |  3
HP:0012324  |  Myeloid leukemia  |  2
HP:0002202  |  Pleural effusion  |  2
HP:0002110  |  Bronchiectasis  |  2
HP:0100279  |  Ulcerative colitis  |  2
HP:0002721  |  Immunodeficiency  |  2
HP:0001945  |  Fever  |  2
HP:0006721  |  Acute lymphocytic leukemia  |  2
HP:0012115  |  Liver inflammation  |  1
HP:0002633  |  Vasculitis  |  1
HP:0002113  |  Pulmonary infiltrates  |  1
HP:0005945  |  Laryngeal obstruction  |  1
HP:0002665  |  Lymphoma  |  1
HP:0005584  |  Renal cell carcinoma  |  1
HP:0002789  |  Increased respiratory rate or depth of breathing  |  1
HP:0100570  |  Carcinoid tumor  |  1
HP:0001369  |  Arthritis  |  1
HP:0001394  |  Hepatic cirrhosis  |  1
HP:0005521  |  Disseminated intravascular coagulation  |  1
HP:0012486  |  Inflammation of spinal cord  |  1
HP:0006000  |  Ureteral obstruction  |  1
HP:0002239  |  Gastrointestinal hemorrhage  |  1
HP:0001903  |  Anemia  |  1
HP:0100523  |  Hepatic abscess  |  1
HP:0006698  |  Ventricular aneurysm  |  1
HP:0001297  |  Cerebral vascular events  |  1
HP:0012189  |  Hodgkin disease  |  1
HP:0006775  |  Multiple myeloma  |  1
HP:0100626  |  Chronic hepatic failure  |  1
HP:0000752  |  Hyperactive behavior  |  1
HP:0100727  |  Histiocytosis  |  1
HP:0002584  |  Intestinal hemorrhage  |  1
HP:0009733  |  Glioma  |  1
HP:0002410  |  Aqueductal stenosis  |  1
HP:0002779  |  Tracheomalacia  |  1
HP:0005550  |  Chronic lymphatic leukemia  |  1
HP:0002138  |  Subarachnoid hemorrhage  |  1
HP:0002094  |  Dyspnea  |  1
HP:0001915  |  Aplastic anemia  |  1
HP:0200036  |  Skin nodule  |  1
HP:0002583  |  Colitis  |  1
HP:0011945  |  Cryptogenic organizing pneumonia  |  1
HP:0007824  |  Total ophthalmoplegia  |  1
HP:0001396  |  Cholestasis  |  1
HP:0001681  |  Angina pectoris  |  1
HP:0012234  |  Agranulocytosis  |  1
HP:0002617  |  Aneurysmal dilatation  |  1
HP:0012653  |  Acute severe asthma  |  1
HP:0012539  |  Non-Hodgkin lymphoma  |  1
HP:0000246  |  Sinus inflammation  |  1
HP:0001370  |  Rheumatoid arthritis  |  1
Disease ID 928
Disease aspergillosis
Manually Symptom
UMLS  | Name(Total Manually Symptoms:26)
C2707258  |  infections
C2364133  |  infection
C1963154  |  renal failure
C1739376  |  orbital apex syndrome
C1546533  |  abscess
C1510428  |  cerebral abscess
C1298681  |  oxalosis
C0748159  |  pulmonary involvement
C0333040  |  fungus ball
C0302148  |  thrombus
C0265149  |  purulent pericarditis
C0264265  |  nasal necrosis
C0259737  |  adiaspiromycosis
C0241950  |  bowel infarction
C0238790  |  bone destruction
C0238036  |  bronchocentric granulomatosis
C0149711  |  hilar adenopathy
C0030486  |  paraplegia
C0029132  |  optic neuropathy
C0029089  |  ophthalmoplegia
C0028992  |  omphalitis
C0025289  |  meningitis
C0024894  |  mastitis
C0019655  |  histoplasmosis
C0019079  |  haemoptysis
C0014556  |  psychomotor seizure
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:5)
C0009450  |  infection  |  13
C0021311  |  infections  |  3
C0333040  |  fungus ball  |  2
C1739376  |  orbital apex syndrome  |  1
C0748159  |  pulmonary involvement  |  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:0)
(Waiting for update.)
Mapped by homologous gene(Total Items:0)
(Waiting for update.)
Disease ID 928
Disease aspergillosis
Case(Waiting for update.)