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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine



   cryptococcosis
  

Disease ID 987
Disease cryptococcosis
Definition
Infection with a fungus of the species CRYPTOCOCCUS NEOFORMANS.
Synonym
(cryptococcosis [& european]) or (torula) or (busse buschkes disease)
(cryptococcosis [& european]) or (torula) or (busse buschkes disease) (disorder)
[x]cryptococcosis, unspecified
[x]cryptococcosis, unspecified (disorder)
busse - buschke's disease
busse-buschke disease
busse-buschke's disease
cryptococcoses
cryptococcosis (disorder)
cryptococcosis [disease/finding]
cryptococcosis nos
cryptococcosis nos (disorder)
cryptococcosis, nos
cryptococcus infection neoformans
cryptococcus neoformans
european blastomycosis
european cryptococcosis
infection by cryptococcus neoformans
torula
toruloses
torulosis
Orphanet
DOID
UMLS
C0010414
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:66)
C0025289  |  meningitis  |  10
C0025309  |  meningoencephalitis  |  5
C0010346  |  crohn's disease  |  4
C0085436  |  cryptococcal meningitis  |  4
C0029443  |  osteomyelitis  |  3
C0026946  |  fungal infection  |  3
C0010414  |  cryptococcosis  |  3
C0010414  |  cryptococcus neoformans  |  3
C0026946  |  fungal infections  |  3
C0041296  |  tuberculosis  |  2
C0024299  |  lymphoma  |  2
C0276688  |  cryptococcal pneumonia  |  2
C0024141  |  systemic lupus erythematosus  |  2
C0023890  |  cirrhosis  |  2
C0023418  |  leukemia  |  2
C0007117  |  basal cell carcinoma  |  2
C0019829  |  hodgkin lymphoma  |  1
C0015645  |  fasciitis  |  1
C0043092  |  wegener's granulomatosis  |  1
C0206138  |  crest syndrome  |  1
C0040034  |  thrombocytopenia  |  1
C0553576  |  systemic fungal infection  |  1
C0007642  |  cellulitis  |  1
C0002871  |  anemia  |  1
C0019158  |  hepatitis  |  1
C0241910  |  autoimmune hepatitis  |  1
C0003873  |  rheumatoid arthritis  |  1
C0019196  |  hepatitis c  |  1
C0553576  |  systemic mycosis  |  1
C0024115  |  lung disease  |  1
C0206744  |  cd4+ t lymphocytopenia  |  1
C0085110  |  severe combined immunodeficiency  |  1
C1961099  |  t-cell acute lymphoblastic leukemia  |  1
C0001175  |  acquired immune deficiency syndrome  |  1
C1565489  |  renal insufficiency  |  1
C0006272  |  bronchiolitis obliterans  |  1
C0026769  |  multiple sclerosis  |  1
C0031154  |  peritonitis  |  1
C0024205  |  lymphadenitis  |  1
C0014060  |  encephalitis c  |  1
C0027813  |  neuritis  |  1
C0011849  |  diabetes mellitus  |  1
C0409974  |  lupus erythematosus  |  1
C0031036  |  polyarteritis nodosa  |  1
C0001973  |  alcoholism  |  1
C0206744  |  idiopathic cd4+ t lymphocytopenia  |  1
C0238124  |  necrotizing fasciitis  |  1
C0011847  |  diabetes  |  1
C0242770  |  bronchiolitis obliterans organizing pneumonia  |  1
C0006271  |  bronchiolitis  |  1
C0026946  |  mycosis  |  1
C0041327  |  pulmonary tuberculosis  |  1
C0085669  |  acute leukemia  |  1
C0029134  |  optic neuritis  |  1
C0036202  |  sarcoidosis  |  1
C0023448  |  lymphoblastic leukemia  |  1
C0024299  |  malignant lymphoma  |  1
C0042769  |  virus infection  |  1
C0032305  |  pneumocystis  |  1
C0027726  |  nephrotic syndrome  |  1
C0085110  |  severe combined immunodefic  |  1
C0023449  |  acute lymphoblastic leukemia  |  1
C0021874  |  intracranial abscess  |  1
C0015230  |  rash  |  1
C0001623  |  adrenal insufficiency  |  1
C0001175  |  acquired immune deficiency  |  1
Curated Gene(Waiting for update.)
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:3)
2212  |  FCGR2A  |  CIPHER
2214  |  FCGR3A  |  CIPHER
2215  |  FCGR3B  |  CIPHER
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:80)
302  |  ANXA2  |  1.458  |  DISEASES
51107  |  APH1A  |  1.389  |  DISEASES
383  |  ARG1  |  2.481  |  DISEASES
419  |  ART3  |  2.563  |  DISEASES
57673  |  BEND3  |  2.13  |  DISEASES
728  |  C5AR1  |  1.873  |  DISEASES
766  |  CA7  |  1.038  |  DISEASES
801  |  CALM1  |  2.234  |  DISEASES
64170  |  CARD9  |  3.333  |  DISEASES
388372  |  CCL4L1  |  2.211  |  DISEASES
6354  |  CCL7  |  2.092  |  DISEASES
958  |  CD40  |  2.234  |  DISEASES
959  |  CD40LG  |  2.808  |  DISEASES
960  |  CD44  |  1.364  |  DISEASES
942  |  CD86  |  2.917  |  DISEASES
1038  |  CDR1  |  1.014  |  DISEASES
94027  |  CGB7  |  4.428  |  DISEASES
94115  |  CGB8  |  4.332  |  DISEASES
27159  |  CHIA  |  1.398  |  DISEASES
93978  |  CLEC6A  |  2.542  |  DISEASES
1259  |  CNGA1  |  2.34  |  DISEASES
1260  |  CNGA2  |  2.643  |  DISEASES
51428  |  DDX41  |  1.948  |  DISEASES
22894  |  DIS3  |  2.086  |  DISEASES
954  |  ENTPD2  |  1.648  |  DISEASES
377841  |  ENTPD8  |  2.305  |  DISEASES
3266  |  ERAS  |  1.832  |  DISEASES
11340  |  EXOSC8  |  2.786  |  DISEASES
2213  |  FCGR2B  |  1.43  |  DISEASES
2214  |  FCGR3A  |  1.547  |  DISEASES
2318  |  FLNC  |  1.163  |  DISEASES
2517  |  FUCA1  |  1.794  |  DISEASES
29933  |  GPR132  |  1.016  |  DISEASES
2877  |  GPX2  |  1.224  |  DISEASES
3198  |  HOXA1  |  1.835  |  DISEASES
3586  |  IL10  |  2.888  |  DISEASES
3605  |  IL17A  |  3.004  |  DISEASES
3652  |  IPP  |  1.199  |  DISEASES
3664  |  IRF6  |  1.268  |  DISEASES
3684  |  ITGAM  |  3.018  |  DISEASES
6453  |  ITSN1  |  1.986  |  DISEASES
3776  |  KCNK2  |  1.349  |  DISEASES
3932  |  LCK  |  1.415  |  DISEASES
8825  |  LIN7A  |  1.971  |  DISEASES
3996  |  LLGL1  |  1.146  |  DISEASES
9361  |  LONP1  |  1.446  |  DISEASES
4153  |  MBL2  |  1.606  |  DISEASES
57591  |  MKL1  |  1.107  |  DISEASES
4615  |  MYD88  |  2.122  |  DISEASES
4843  |  NOS2  |  1.623  |  DISEASES
56953  |  NT5M  |  1.273  |  DISEASES
390874  |  ONECUT3  |  1.863  |  DISEASES
5089  |  PBX2  |  2.051  |  DISEASES
5328  |  PLAU  |  1.451  |  DISEASES
5329  |  PLAUR  |  1.032  |  DISEASES
151056  |  PLB1  |  4.057  |  DISEASES
9677  |  PPIP5K1  |  2.227  |  DISEASES
5530  |  PPP3CA  |  1.164  |  DISEASES
5788  |  PTPRC  |  1.22  |  DISEASES
6189  |  RPS3A  |  1.665  |  DISEASES
6281  |  S100A10  |  2.287  |  DISEASES
6441  |  SFTPD  |  1.65  |  DISEASES
9467  |  SH3BP5  |  1.099  |  DISEASES
23583  |  SMUG1  |  2.788  |  DISEASES
400410  |  ST20  |  2.586  |  DISEASES
6772  |  STAT1  |  1.686  |  DISEASES
6776  |  STAT5A  |  1.375  |  DISEASES
8576  |  STK16  |  3.991  |  DISEASES
8428  |  STK24  |  1.223  |  DISEASES
6905  |  TBCE  |  1.367  |  DISEASES
7099  |  TLR4  |  2.083  |  DISEASES
54106  |  TLR9  |  2.222  |  DISEASES
7124  |  TNF  |  2.876  |  DISEASES
8764  |  TNFRSF14  |  1.095  |  DISEASES
7293  |  TNFRSF4  |  1.605  |  DISEASES
9094  |  UNC119  |  3.874  |  DISEASES
6293  |  VPS52  |  2.254  |  DISEASES
22803  |  XRN2  |  2.493  |  DISEASES
7549  |  ZNF2  |  4.477  |  DISEASES
148266  |  ZNF569  |  1.809  |  DISEASES
Locus(Waiting for update.)
Disease ID 987
Disease cryptococcosis
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:48)
HP:0006532  |  Pneumonia, recurrent episodes  |  10
HP:0001287  |  Meningitis  |  10
HP:0002721  |  Immunodeficiency  |  5
HP:0100280  |  Morbus Crohn  |  4
HP:0002754  |  Bone infection  |  4
HP:0001880  |  Eosinophilia  |  2
HP:0002725  |  Systemic lupus erythematosus  |  2
HP:0001945  |  Fever  |  2
HP:0002671  |  Basalioma  |  2
HP:0002665  |  Lymphoma  |  2
HP:0011450  |  CNS infection  |  2
HP:0001394  |  Hepatic cirrhosis  |  2
HP:0001909  |  Leukemia  |  2
HP:0008940  |  Generalized lymphadenopathy  |  1
HP:0100754  |  Mania  |  1
HP:0012735  |  Coughing  |  1
HP:0000083  |  Renal insufficiency  |  1
HP:0100658  |  Bacterial infection of skin  |  1
HP:0006721  |  Acute lymphocytic leukemia  |  1
HP:0002840  |  Lymphadenitis  |  1
HP:0000572  |  Visual loss  |  1
HP:0100537  |  Inflammation of the fascia  |  1
HP:0002202  |  Pleural effusion  |  1
HP:0004430  |  Severe combined immunodeficiency  |  1
HP:0000819  |  Diabetes mellitus  |  1
HP:0011950  |  Bronchiolitis  |  1
HP:0030731  |  Carcinoma  |  1
HP:0005403  |  Decreased numbers of circulating T cells  |  1
HP:0005387  |  Combined immunodeficiency  |  1
HP:0100653  |  Optic neuritis  |  1
HP:0000846  |  Hypoadrenalism  |  1
HP:0012189  |  Hodgkin disease  |  1
HP:0002102  |  Pleuritis  |  1
HP:0001370  |  Rheumatoid arthritis  |  1
HP:0002716  |  Lymph node hyperplasia  |  1
HP:0001888  |  Lymphocytopenia  |  1
HP:0001903  |  Anemia  |  1
HP:0012115  |  Liver inflammation  |  1
HP:0001873  |  Low platelet count  |  1
HP:0012190  |  T cell lymphoma  |  1
HP:0002719  |  infections, recurrent  |  1
HP:0000100  |  Nephrosis  |  1
HP:0100721  |  Mediastinal lymphadenopathy  |  1
HP:0002955  |  Granulomatosis  |  1
HP:0002586  |  Peritonitis  |  1
HP:0011946  |  Constrictive bronchiolitis  |  1
HP:0002488  |  Acute leukemias  |  1
HP:0011945  |  Cryptogenic organizing pneumonia  |  1
Disease ID 987
Disease cryptococcosis
Manually Symptom
UMLS  | Name(Total Manually Symptoms:10)
C2029884  |  hearing loss
C1963059  |  adrenal insufficiency
C1840264  |  immune suppression
C1619738  |  immune reconstitution inflammatory syndrome
C0264490  |  acute respiratory failure
C0221505  |  brain lesions
C0155288  |  papilloedema
C0032227  |  pleural effusions
C0031128  |  peripheral vestibular disease
C0019829  |  hodgkin's disease
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:11)
C0009450  |  infection  |  29
C0876973  |  pulmonary infection  |  9
C0025289  |  meningitis  |  8
C0025309  |  meningoencephalitis  |  6
C0021311  |  infections  |  5
C0029443  |  osteomyelitis  |  4
C0010414  |  cryptococcosis  |  3
C1619738  |  immune reconstitution inflammatory syndrome  |  2
C0026946  |  fungal infections  |  1
C0001623  |  adrenal insufficiency  |  1
C0007642  |  cellulitis  |  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 987
Disease cryptococcosis
Case(Waiting for update.)