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PedAM

Pediatric Disease Annotations & Medicines



   coccidioidomycosis
  

Disease ID 766
Disease coccidioidomycosis
Definition
Infection with a fungus of the genus COCCIDIOIDES, endemic to the SOUTHWESTERN UNITED STATES. It is sometimes called valley fever but should not be confused with RIFT VALLEY FEVER. Infection is caused by inhalation of airborne, fungal particles known as arthroconidia, a form of FUNGAL SPORES. A primary form is an acute, benign, self-limited respiratory infection. A secondary form is a virulent, severe, chronic, progressive granulomatous disease with systemic involvement. It can be detected by use of COCCIDIOIDIN.
Synonym
[x]coccidioidomycosis, unspecified
[x]coccidioidomycosis, unspecified (disorder)
coccidioides immitis infection
coccidioides immitis infections
coccidioidomycoses
coccidioidomycosis (disorder)
coccidioidomycosis [disease/finding]
coccidioidomycosis infection
coccidioidomycosis nos
coccidioidomycosis nos (disorder)
coccidioidomycosis, nos
coccidioidomycosis, unspecified
desert fever
disease posada wernicke
fever, desert
fever, san joaquin
fever, valley
infection by coccidioides immitis
infection by coccidioides immitis (disorder)
infection caused by coccidioides immitis
infection caused by coccidioides immitis (disorder)
infection, coccidioides immitis
infections, coccidioides immitis
posadas-wernicke disease
san joaquin valley fever
valley fever
valley fevers
Orphanet
DOID
ICD10
UMLS
C0009186
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:4)
C0029443  |  osteomyelitis  |  2
C0026946  |  fungal infection  |  1
C0026946  |  fungal infections  |  1
C0005716  |  blastomycosis  |  1
Curated Gene(Waiting for update.)
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:55)
1595  |  CYP51A1  |  DISEASES
4282  |  MIF  |  DISEASES
2954  |  GSTZ1  |  DISEASES
3558  |  IL2  |  DISEASES
969  |  CD69  |  DISEASES
51561  |  IL23A  |  DISEASES
3458  |  IFNG  |  DISEASES
3565  |  IL4  |  DISEASES
3567  |  IL5  |  DISEASES
3554  |  IL1R1  |  DISEASES
4953  |  ODC1  |  DISEASES
4360  |  MRC1  |  DISEASES
654231  |  OCM  |  DISEASES
30833  |  NT5C  |  DISEASES
5199  |  CFP  |  DISEASES
325  |  APCS  |  DISEASES
4951  |  OCM2  |  DISEASES
3569  |  IL6  |  DISEASES
7097  |  TLR2  |  DISEASES
4591  |  TRIM37  |  DISEASES
3552  |  IL1A  |  DISEASES
3553  |  IL1B  |  DISEASES
5741  |  PTH  |  DISEASES
2911  |  GRM1  |  DISEASES
85451  |  UNK  |  DISEASES
27306  |  HPGDS  |  DISEASES
213  |  ALB  |  DISEASES
64581  |  CLEC7A  |  DISEASES
5897  |  RAG2  |  DISEASES
6097  |  RORC  |  DISEASES
29933  |  GPR132  |  DISEASES
1538  |  CYLC1  |  DISEASES
3605  |  IL17A  |  DISEASES
3005  |  H1F0  |  DISEASES
6993  |  DYNLT1  |  DISEASES
3459  |  IFNGR1  |  DISEASES
51175  |  TUBE1  |  DISEASES
959  |  CD40LG  |  DISEASES
51013  |  EXOSC1  |  DISEASES
64170  |  CARD9  |  DISEASES
5476  |  CTSA  |  DISEASES
7099  |  TLR4  |  DISEASES
3561  |  IL2RG  |  DISEASES
57134  |  MAN1C1  |  DISEASES
1192  |  CLIC1  |  DISEASES
7133  |  TNFRSF1B  |  DISEASES
1536  |  CYBB  |  DISEASES
5077  |  PAX3  |  DISEASES
1638  |  DCT  |  DISEASES
26013  |  L3MBTL1  |  DISEASES
7124  |  TNF  |  DISEASES
4615  |  MYD88  |  DISEASES
7555  |  CNBP  |  DISEASES
3586  |  IL10  |  DISEASES
83695  |  RHNO1  |  DISEASES
Locus(Waiting for update.)
Disease ID 766
Disease coccidioidomycosis
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:7)
Disease ID 766
Disease coccidioidomycosis
Manually Symptom
UMLS  | Name(Total Manually Symptoms:20)
C2364051  |  fatigue
C2240374  |  eosinophilia
C2073625  |  pleural effusion
C1710146  |  spinal arachnoiditis
C1555769  |  pulmonary disease
C1550639  |  fistula
C1546654  |  granuloma
C0740852  |  upper airway obstruction
C0497156  |  adenopathy
C0264551  |  exudative pleurisy
C0155862  |  lobar pneumonia
C0154652  |  eosinophilic meningitis
C0037285  |  skin manifestations
C0035333  |  retinitis
C0033581  |  prostatitis
C0032285  |  pneumonia
C0029895  |  otomycosis
C0020437  |  hypercalcemia
C0014743  |  erythema nodosum
C0008512  |  chorioretinal scars
Text Mined Symptom(Waiting for update.)
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:0)
(Waiting for update.)
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)