Home Contact Sitemap

PedAM

Pediatric Disease Annotations & Medicines



   cryptosporidiosis
  

Disease ID 403
Disease cryptosporidiosis
Definition
Intestinal infection with organisms of the genus CRYPTOSPORIDIUM. It occurs in both animals and humans. Symptoms include severe DIARRHEA.
Synonym
cryptosporidiasis
cryptosporidioses
cryptosporidiosis (disorder)
cryptosporidiosis [disease/finding]
cryptosporidium infection
infection by cryptosporidium
infection by cryptosporidium (disorder)
infection by cryptosporidium, nos
infection caused by cryptosporidium
infection caused by cryptosporidium (disorder)
intestinal cryptosporidiosis
Orphanet
DOID
ICD10
UMLS
C0010418
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:25)
C0011991  |  diarrhea  |  7
C0007113  |  rectal cancer  |  3
C0001175  |  acquired immune deficiency  |  3
C0001175  |  acquired immune deficiency syndrome  |  3
C0009402  |  colorectal cancer  |  3
C0162429  |  malnutrition  |  2
C0001418  |  adenocarcinoma  |  2
C0038012  |  spondylitis  |  1
C0006840  |  candidiasis  |  1
C0030499  |  parasitic diseases  |  1
C0008311  |  cholangitis  |  1
C0001175  |  acquired immune deficiency syndrome (aids)  |  1
C0023449  |  acute lymphoblastic leukemia  |  1
C0001175  |  acquired immunodeficiency syndrome  |  1
C0267918  |  chronic cholangitis  |  1
C0023418  |  leukemia  |  1
C0178238  |  intestinal infection  |  1
C0007137  |  squamous cell carcinoma  |  1
C0023448  |  lymphoblastic leukemia  |  1
C0038013  |  ankylosing spondylitis  |  1
C0017536  |  giardiasis  |  1
C0024523  |  malabsorption  |  1
C0011991  |  diarrhoea  |  1
C0919659  |  oropharyngeal candidiasis  |  1
C0030499  |  parasitic disease  |  1
Curated Gene(Waiting for update.)
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:1)
4153  |  MBL2  |  infer
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:96)
3566  |  IL4R  |  DISEASES
23505  |  TMEM131  |  DISEASES
191  |  AHCY  |  DISEASES
1158  |  CKM  |  DISEASES
973  |  CD79A  |  DISEASES
8976  |  WASL  |  DISEASES
3558  |  IL2  |  DISEASES
3458  |  IFNG  |  DISEASES
7167  |  TPI1  |  DISEASES
3565  |  IL4  |  DISEASES
3273  |  HRG  |  DISEASES
7291  |  TWIST1  |  DISEASES
55821  |  ALLC  |  DISEASES
55902  |  ACSS2  |  DISEASES
1965  |  EIF2S1  |  DISEASES
6505  |  SLC1A1  |  DISEASES
25939  |  SAMHD1  |  DISEASES
10552  |  ARPC1A  |  DISEASES
55850  |  USE1  |  DISEASES
3938  |  LCT  |  DISEASES
7294  |  TXK  |  DISEASES
8452  |  CUL3  |  DISEASES
80725  |  SRCIN1  |  DISEASES
6550  |  SLC9A3  |  DISEASES
23534  |  TNPO3  |  DISEASES
23395  |  LARS2  |  DISEASES
3687  |  ITGAX  |  DISEASES
740  |  MRPL49  |  DISEASES
9453  |  GGPS1  |  DISEASES
29028  |  ATAD2  |  DISEASES
6750  |  SST  |  DISEASES
5739  |  PTGIR  |  DISEASES
9437  |  NCR1  |  DISEASES
10109  |  ARPC2  |  DISEASES
64789  |  EXO5  |  DISEASES
5267  |  SERPINA4  |  DISEASES
7083  |  TK1  |  DISEASES
3308  |  HSPA4  |  DISEASES
79071  |  ELOVL6  |  DISEASES
8419  |  BFSP2  |  DISEASES
7386  |  UQCRFS1  |  DISEASES
57521  |  RPTOR  |  DISEASES
5187  |  PER1  |  DISEASES
998  |  CDC42  |  DISEASES
7298  |  TYMS  |  DISEASES
4261  |  CIITA  |  DISEASES
5551  |  PRF1  |  DISEASES
53347  |  UBASH3A  |  DISEASES
6863  |  TAC1  |  DISEASES
6181  |  RPLP2  |  DISEASES
1670  |  DEFA5  |  DISEASES
92335  |  STRADA  |  DISEASES
1058  |  CENPA  |  DISEASES
9138  |  ARHGEF1  |  DISEASES
5313  |  PKLR  |  DISEASES
132884  |  EVC2  |  DISEASES
2873  |  GPS1  |  DISEASES
2224  |  FDPS  |  DISEASES
9652  |  TTC37  |  DISEASES
58484  |  NLRC4  |  DISEASES
7432  |  VIP  |  DISEASES
6375  |  XCL1  |  DISEASES
5654  |  HTRA1  |  DISEASES
959  |  CD40LG  |  DISEASES
81030  |  ZBP1  |  DISEASES
6015  |  RING1  |  DISEASES
58496  |  LY6G5B  |  DISEASES
1460  |  CSNK2B  |  DISEASES
55937  |  APOM  |  DISEASES
6564  |  SLC15A1  |  DISEASES
2017  |  CTTN  |  DISEASES
11074  |  TRIM31  |  DISEASES
6103  |  RPGR  |  DISEASES
3980  |  LIG3  |  DISEASES
1646  |  AKR1C2  |  DISEASES
1645  |  AKR1C1  |  DISEASES
4267  |  CD99  |  DISEASES
752014  |  CEMP1  |  DISEASES
7520  |  XRCC5  |  DISEASES
9560  |  CCL4L2  |  DISEASES
64115  |  C10orf54  |  DISEASES
4357  |  MPST  |  DISEASES
344022  |  NOTO  |  DISEASES
1719  |  DHFR  |  DISEASES
7124  |  TNF  |  DISEASES
3586  |  IL10  |  DISEASES
51071  |  DERA  |  DISEASES
2649  |  NR6A1  |  DISEASES
2994  |  GYPB  |  DISEASES
1622  |  DBI  |  DISEASES
4850  |  CNOT4  |  DISEASES
54937  |  SOHLH2  |  DISEASES
820  |  CAMP  |  DISEASES
11201  |  POLI  |  DISEASES
246734  |  NPCDR1  |  DISEASES
378805  |  LINC-PINT  |  DISEASES
Locus(Waiting for update.)
Disease ID 403
Disease cryptosporidiosis
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:13)
HP:0002014  |  Diarrhea  |  7
HP:0002721  |  Immunodeficiency  |  5
HP:0001824  |  Weight loss  |  4
HP:0004395  |  Malnutrition  |  2
HP:0001944  |  Dehydration  |  2
HP:0002013  |  Emesis  |  1
HP:0006721  |  Acute lymphocytic leukemia  |  1
HP:0030151  |  Cholangitis  |  1
HP:0001508  |  Weight faltering  |  1
HP:0002024  |  Intestinal malabsorption  |  1
HP:0001263  |  Developmental retardation  |  1
HP:0001909  |  Leukemia  |  1
HP:0002860  |  Squamous cell carcinoma  |  1
Disease ID 403
Disease cryptosporidiosis
Manually Symptom
UMLS  | Name(Total Manually Symptoms:14)
C2707258  |  infections
C1963165  |  malabsorption
C1963091  |  diarrhea
C1963083  |  cholecystitis
C1443924  |  severe diarrhoea
C0859865  |  aural polyp
C0520571  |  biliary fibrosis
C0275708  |  mycobacterium marinum infection
C0267557  |  secretory diarrhea
C0156272  |  enterovesical fistula
C0025162  |  toxic megacolon
C0024523  |  malabsorption syndrome
C0011991  |  diarrhoea
C0006285  |  bronchopneumonia
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:4)
C0011991  |  diarrhea  |  7
C0021311  |  infections  |  4
C0011991  |  diarrhoea  |  1
C0024523  |  malabsorption  |  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: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.)