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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine



   cysticercosis
  

Disease ID 1236
Disease cysticercosis
Definition
Infection with CYSTICERCUS, the larval form of the various tapeworms of the genus Taenia (usually T. solium in man). In humans they penetrate the intestinal wall and invade subcutaneous tissue, brain, eye, muscle, heart, liver, lung, and peritoneum. Brain involvement results in NEUROCYSTICERCOSIS.
Synonym
[x]cysticercosis, unspecified
[x]cysticercosis, unspecified (disorder)
cysticerciasis
cysticercoses
cysticercosis (disorder)
cysticercosis [disease/finding]
infection by tapeworm larvae
infection by tapeworm larvae (disorder)
infection caused by tapeworm larvae
infection caused by tapeworm larvae (disorder)
larval taeniasis
larval tapeworm infection
larval teniasis
Orphanet
DOID
UMLS
C0010678
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:16)
C0014544  |  epilepsy  |  5
C0039254  |  taeniasis  |  3
C0014556  |  temporal lobe epilepsy  |  1
C0027765  |  neurological disorder  |  1
C0456909  |  vision loss  |  1
C0027765  |  neurological disorders  |  1
C0042075  |  urological disorders  |  1
C0020255  |  hydrocephalus  |  1
C0017601  |  glaucoma  |  1
C0014544  |  epileptic seizure  |  1
C0037280  |  infestation  |  1
C0014544  |  epileptic seizures  |  1
C0005745  |  ptosis  |  1
C0042165  |  anterior uveitis  |  1
C0017609  |  neovascular glaucoma  |  1
C0042164  |  uveitis  |  1
Curated Gene(Waiting for update.)
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:73)
273  |  AMPH  |  1.096  |  DISEASES
383  |  ARG1  |  2.382  |  DISEASES
142686  |  ASB14  |  3.85  |  DISEASES
7917  |  BAG6  |  1.351  |  DISEASES
811  |  CALR  |  2.932  |  DISEASES
930  |  CD19  |  1.325  |  DISEASES
29126  |  CD274  |  1.71  |  DISEASES
959  |  CD40LG  |  3.245  |  DISEASES
1066  |  CES1  |  1.25  |  DISEASES
9244  |  CRLF1  |  2.139  |  DISEASES
1544  |  CYP1A2  |  1.28  |  DISEASES
51428  |  DDX41  |  1.697  |  DISEASES
1810  |  DR1  |  1.482  |  DISEASES
79813  |  EHMT1  |  1.774  |  DISEASES
23741  |  EID1  |  1.93  |  DISEASES
255324  |  EPGN  |  1.278  |  DISEASES
2172  |  FABP6  |  2.022  |  DISEASES
2266  |  FGG  |  1.721  |  DISEASES
2316  |  FLNA  |  1.189  |  DISEASES
50943  |  FOXP3  |  1.571  |  DISEASES
29933  |  GPR132  |  2.171  |  DISEASES
9446  |  GSTO1  |  2.644  |  DISEASES
81502  |  HM13  |  1.87  |  DISEASES
3586  |  IL10  |  2.875  |  DISEASES
29949  |  IL19  |  1.397  |  DISEASES
3608  |  ILF2  |  2.348  |  DISEASES
3684  |  ITGAM  |  1.076  |  DISEASES
102723508  |  KANTR  |  1.361  |  DISEASES
987  |  LRBA  |  1.056  |  DISEASES
4065  |  LY75  |  1.455  |  DISEASES
4063  |  LY9  |  2.065  |  DISEASES
10046  |  MAMLD1  |  1.85  |  DISEASES
4190  |  MDH1  |  2.045  |  DISEASES
79104  |  MEG8  |  1.076  |  DISEASES
4318  |  MMP9  |  1.986  |  DISEASES
4512  |  MT-CO1  |  5.103  |  DISEASES
4519  |  MT-CYB  |  2.627  |  DISEASES
4535  |  MT-ND1  |  3.655  |  DISEASES
4948  |  OCA2  |  1.149  |  DISEASES
80380  |  PDCD1LG2  |  2.46  |  DISEASES
11331  |  PHB2  |  1.377  |  DISEASES
10957  |  PNRC1  |  2.211  |  DISEASES
5499  |  PPP1CA  |  1.815  |  DISEASES
5730  |  PTGDS  |  1.071  |  DISEASES
26278  |  SACS  |  1.354  |  DISEASES
51150  |  SDF4  |  1.035  |  DISEASES
64218  |  SEMA4A  |  2.149  |  DISEASES
9467  |  SH3BP5  |  2.298  |  DISEASES
51100  |  SH3GLB1  |  2.768  |  DISEASES
114836  |  SLAMF6  |  1.903  |  DISEASES
89886  |  SLAMF9  |  4.255  |  DISEASES
788  |  SLC25A20  |  1.597  |  DISEASES
91137  |  SLC25A46  |  1.694  |  DISEASES
114798  |  SLITRK1  |  1.091  |  DISEASES
139886  |  SPIN4  |  3.807  |  DISEASES
503542  |  SPRN  |  1.705  |  DISEASES
6815  |  STYX  |  2.96  |  DISEASES
6863  |  TAC1  |  2.104  |  DISEASES
4070  |  TACSTD2  |  3.719  |  DISEASES
7053  |  TGM3  |  1.281  |  DISEASES
7099  |  TLR4  |  2.588  |  DISEASES
54106  |  TLR9  |  1.003  |  DISEASES
7124  |  TNF  |  2.155  |  DISEASES
8794  |  TNFRSF10C  |  2.256  |  DISEASES
8784  |  TNFRSF18  |  1.025  |  DISEASES
9760  |  TOX  |  1.072  |  DISEASES
7169  |  TPM2  |  1.722  |  DISEASES
51592  |  TRIM33  |  1.666  |  DISEASES
7295  |  TXN  |  1.863  |  DISEASES
114112  |  TXNRD3  |  3.51  |  DISEASES
51366  |  UBR5  |  2.783  |  DISEASES
91544  |  UBXN11  |  3.262  |  DISEASES
10269  |  ZMPSTE24  |  1.542  |  DISEASES
Locus(Waiting for update.)
Disease ID 1236
Disease cysticercosis
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:17)
HP:0002315  |  Headaches  |  2
HP:0009733  |  Glioma  |  1
HP:0002633  |  Vasculitis  |  1
HP:0000554  |  Uveitis  |  1
HP:0001250  |  Seizures  |  1
HP:0007902  |  Vitreous hemorrhage  |  1
HP:0000572  |  Visual loss  |  1
HP:0011450  |  CNS infection  |  1
HP:0200026  |  Ocular pain  |  1
HP:0012122  |  Anterior uveitis  |  1
HP:0002617  |  Aneurysmal dilatation  |  1
HP:0000501  |  Glaucoma  |  1
HP:0002664  |  Neoplasia  |  1
HP:0001257  |  Spasticity  |  1
HP:0000238  |  Nonsyndromal hydrocephalus  |  1
HP:0000508  |  Drooping upper eyelid  |  1
HP:0012531  |  Pain  |  1
Disease ID 1236
Disease cysticercosis
Manually Symptom
UMLS  | Name(Total Manually Symptoms:14)
C2364133  |  infection
C1963137  |  hydrocephalus
C1384353  |  infestation
C0796095  |  c syndrome
C0522224  |  palsy
C0260662  |  hearing disorders
C0234978  |  jacksonian epilepsy
C0221505  |  cerebral lesions
C0149507  |  orbital cellulitis
C0042373  |  vascular disorders
C0033377  |  ptosis
C0026848  |  myopathy
C0014544  |  epileptic fits
C0014038  |  encephalitis
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:4)
C0009450  |  infection  |  5
C0037280  |  infestation  |  1
C0005745  |  ptosis  |  1
C0020255  |  hydrocephalus  |  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 1236
Disease cysticercosis
Case(Waiting for update.)