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Pediatric Disease Annotations & Medicines



   histoplasmosis
  

Disease ID 443
Disease histoplasmosis
Definition
Infection resulting from inhalation or ingestion of spores of the fungus of the genus HISTOPLASMA, species H. capsulatum. It is worldwide in distribution and particularly common in the midwestern United States. (From Dorland, 27th ed)
Synonym
[x]histoplasmosis, unspecified
[x]histoplasmosis, unspecified (disorder)
histoplasmoses
histoplasmosis (disorder)
histoplasmosis [disease/finding]
histoplasmosis nos
histoplasmosis, nos
histoplasmosis, unspecified
unspecified histoplasmosis infection
unspecified histoplasmosis infection (disorder)
unspecified histoplasmosis nos
unspecified histoplasmosis nos (disorder)
Orphanet
DOID
ICD10
UMLS
C0019655
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:38)
C0001175  |  acquired immunodeficiency syndrome  |  3
C0009319  |  colitis  |  2
C0006840  |  candidiasis  |  2
C0024291  |  hemophagocytic lymphohistiocytosis  |  2
C0020437  |  hypercalcemia  |  2
C0025064  |  mediastinitis  |  2
C0022398  |  job's syndrome  |  1
C0032231  |  pleuritis  |  1
C0006625  |  cachexia  |  1
C0014742  |  erythema multiforme  |  1
C0023281  |  leishmaniasis  |  1
C0023351  |  tuberculoid leprosy  |  1
C0037274  |  dermatosis  |  1
C0027947  |  neutropenia  |  1
C0027707  |  interstitial nephritis  |  1
C0027697  |  nephritis  |  1
C0023290  |  visceral leishmaniasis  |  1
C0042164  |  uveitis  |  1
C0030312  |  pancytopenia  |  1
C0033860  |  psoriasis  |  1
C0010346  |  crohn's disease  |  1
C0041296  |  tuberculosis  |  1
C0024141  |  systemic lupus erythematosus  |  1
C0001403  |  addison's disease  |  1
C0042384  |  vasculitis  |  1
C0085253  |  adult onset still's disease  |  1
C0013370  |  amoebic colitis  |  1
C0023343  |  leprosy  |  1
C0008370  |  cholestasis  |  1
C0024291  |  hemophagocytic syndrome  |  1
C0003708  |  arachnoiditis  |  1
C0003873  |  rheumatoid arthritis  |  1
C0003864  |  arthritis  |  1
C0002874  |  aplastic anemia  |  1
C0036202  |  sarcoidosis  |  1
C0008513  |  chorioretinitis  |  1
C0003872  |  psoriatic arthritis  |  1
C0001175  |  acquired immunodeficiency syndrome (aids)  |  1
Curated Gene(Waiting for update.)
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:93)
1595  |  CYP51A1  |  DISEASES
920  |  CD4  |  DISEASES
55359  |  STYK1  |  DISEASES
10777  |  ARPP21  |  DISEASES
2191  |  FAP  |  DISEASES
3053  |  SERPIND1  |  DISEASES
49  |  ACR  |  DISEASES
2137  |  EXTL3  |  DISEASES
973  |  CD79A  |  DISEASES
3912  |  LAMB1  |  DISEASES
55703  |  POLR3B  |  DISEASES
3458  |  IFNG  |  DISEASES
3565  |  IL4  |  DISEASES
27241  |  BBS9  |  DISEASES
6939  |  TCF15  |  DISEASES
10365  |  KLF2  |  DISEASES
6351  |  CCL4  |  DISEASES
27112  |  FAM155B  |  DISEASES
3958  |  LGALS3  |  DISEASES
27348  |  TOR1B  |  DISEASES
9172  |  MYOM2  |  DISEASES
4591  |  TRIM37  |  DISEASES
27130  |  INVS  |  DISEASES
941  |  CD80  |  DISEASES
5443  |  POMC  |  DISEASES
54847  |  SIDT1  |  DISEASES
8829  |  NRP1  |  DISEASES
3858  |  KRT10  |  DISEASES
523  |  ATP6V1A  |  DISEASES
167410  |  LIX1  |  DISEASES
4715  |  NDUFB9  |  DISEASES
1834  |  DSPP  |  DISEASES
23250  |  ATP11A  |  DISEASES
26059  |  ERC2  |  DISEASES
1636  |  ACE  |  DISEASES
1234  |  CCR5  |  DISEASES
151112  |  ZSWIM2  |  DISEASES
3490  |  IGFBP7  |  DISEASES
213  |  ALB  |  DISEASES
1437  |  CSF2  |  DISEASES
124872  |  B4GALNT2  |  DISEASES
1632  |  ECI1  |  DISEASES
64581  |  CLEC7A  |  DISEASES
2357  |  FPR1  |  DISEASES
56246  |  MRAP  |  DISEASES
1241  |  LTB4R  |  DISEASES
1938  |  EEF2  |  DISEASES
3291  |  HSD11B2  |  DISEASES
3183  |  HNRNPC  |  DISEASES
2318  |  FLNC  |  DISEASES
246329  |  STAC3  |  DISEASES
1538  |  CYLC1  |  DISEASES
25834  |  MGAT4C  |  DISEASES
9094  |  UNC119  |  DISEASES
23583  |  SMUG1  |  DISEASES
3006  |  HIST1H1C  |  DISEASES
3329  |  HSPD1  |  DISEASES
3198  |  HOXA1  |  DISEASES
3605  |  IL17A  |  DISEASES
10516  |  FBLN5  |  DISEASES
80142  |  PTGES2  |  DISEASES
2879  |  GPX4  |  DISEASES
135250  |  RAET1E  |  DISEASES
9652  |  TTC37  |  DISEASES
3459  |  IFNGR1  |  DISEASES
959  |  CD40LG  |  DISEASES
51013  |  EXOSC1  |  DISEASES
6005  |  RHAG  |  DISEASES
7422  |  VEGFA  |  DISEASES
240  |  ALOX5  |  DISEASES
1192  |  CLIC1  |  DISEASES
7133  |  TNFRSF1B  |  DISEASES
3105  |  HLA-A  |  DISEASES
285440  |  CYP4V2  |  DISEASES
1993  |  ELAVL2  |  DISEASES
56953  |  NT5M  |  DISEASES
284217  |  LAMA1  |  DISEASES
3652  |  IPP  |  DISEASES
80380  |  PDCD1LG2  |  DISEASES
10606  |  PAICS  |  DISEASES
7018  |  TF  |  DISEASES
26013  |  L3MBTL1  |  DISEASES
7124  |  TNF  |  DISEASES
3106  |  HLA-B  |  DISEASES
3908  |  LAMA2  |  DISEASES
3594  |  IL12RB1  |  DISEASES
4049  |  LTA  |  DISEASES
54900  |  LAX1  |  DISEASES
3586  |  IL10  |  DISEASES
7019  |  TFAM  |  DISEASES
51428  |  DDX41  |  DISEASES
83695  |  RHNO1  |  DISEASES
6223  |  RPS19  |  DISEASES
Locus(Waiting for update.)
Disease ID 443
Disease histoplasmosis
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:31)
HP:0002721  |  Immunodeficiency  |  6
HP:0002716  |  Lymph node hyperplasia  |  3
HP:0001945  |  Fever  |  3
HP:0003072  |  Hypercalcemia  |  2
HP:0002583  |  Colitis  |  2
HP:0003765  |  Psoriasis  |  1
HP:0002584  |  Intestinal hemorrhage  |  1
HP:0000123  |  Nephritis  |  1
HP:0001396  |  Cholestasis  |  1
HP:0010783  |  Erythema  |  1
HP:0001915  |  Aplastic anemia  |  1
HP:0001370  |  Rheumatoid arthritis  |  1
HP:0001875  |  Neutropenia  |  1
HP:0002725  |  Systemic lupus erythematosus  |  1
HP:0002633  |  Vasculitis  |  1
HP:0001369  |  Arthritis  |  1
HP:0100721  |  Mediastinal lymphadenopathy  |  1
HP:0001876  |  Low blood cell count  |  1
HP:0002239  |  Gastrointestinal hemorrhage  |  1
HP:0008207  |  Addison's disease  |  1
HP:0002102  |  Pleuritis  |  1
HP:0100280  |  Morbus Crohn  |  1
HP:0012156  |  Hemophagocytosis  |  1
HP:0001297  |  Cerebral vascular events  |  1
HP:0012424  |  Chorioretinitis  |  1
HP:0004326  |  Cachexia  |  1
HP:0002094  |  Dyspnea  |  1
HP:0000554  |  Uveitis  |  1
HP:0000105  |  Renal enlargement  |  1
HP:0001970  |  Interstitial nephritis  |  1
HP:0011944  |  Small vessel vasculitis  |  1
Disease ID 443
Disease histoplasmosis
Manually Symptom
UMLS  | Name(Total Manually Symptoms:31)
C2364133  |  infection
C2073625  |  pleural effusion
C1963211  |  pericarditis
C1963059  |  adrenal insufficiency
C1962974  |  chylothorax
C1546654  |  granuloma
C0876973  |  pulmonary infection
C0748168  |  pulmonary pathology
C0456909  |  vision loss
C0340359  |  prosthetic valve endocarditis
C0334121  |  inflammatory myofibroblastic tumor
C0332556  |  coin lesion
C0276648  |  fungal endocarditis
C0240708  |  pericardial calcification
C0235369  |  granulomatous hepatitis
C0221386  |  fibrosing mediastinitis
C0043117  |  idiopathic thrombocytopenic purpura
C0040034  |  thrombocytopenia
C0038833  |  superior vena caval obstruction
C0038833  |  superior vena cava syndrome
C0037285  |  skin manifestations
C0037284  |  skin lesions
C0035243  |  respiratory infection
C0032227  |  pleural effusions
C0030326  |  panniculitis
C0029166  |  oral manifestations
C0024291  |  hemophagocytic syndrome
C0019829  |  hodgkin's disease
C0019825  |  hoarseness
C0007286  |  carpal tunnel syndrome
C0001403  |  addison's disease
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:7)
C0009450  |  infection  |  8
C0037284  |  skin lesions  |  2
C0029166  |  oral manifestations  |  1
C0037285  |  skin manifestations  |  1
C0221386  |  fibrosing mediastinitis  |  1
C0024291  |  hemophagocytic syndrome  |  1
C0001403  |  addison's disease  |  1
Manually Genotype(Total Text Mining 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.)
Chemical(Total Drugs:1)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0019655fluocinolone acetonideD00544667-73-2histoplasmosisMESH:D006660marker/mechanism15767049
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)