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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine



   rabies
  

Disease ID 912
Disease rabies
Definition
Acute VIRAL CNS INFECTION affecting mammals, including humans. It is caused by RABIES VIRUS and usually spread by contamination with virus-laden saliva of bites inflicted by rabid animals. Important animal vectors include the dog, cat, bat, fox, raccoon, skunk, and wolf.
Synonym
[x]rabies, unspecified
[x]rabies, unspecified (disorder)
hydrophobia
hydrophobia (finding)
lyssa
lyssa - rabies
lyssas
rabies (& hydrophobia)
rabies (& hydrophobia) (disorder)
rabies (disorder)
rabies - hydrophobia
rabies [disease/finding]
rabies, nos
Orphanet
DOID
UMLS
C0034494
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:17)
C0027765  |  neurological disease  |  2
C0034494  |  hydrophobia  |  2
C0034494  |  rabies  |  2
C0019348  |  herpes simplex  |  1
C0013884  |  lymphatic filariasis  |  1
C0038362  |  stomatitis  |  1
C0042075  |  urological disorders  |  1
C0014742  |  erythema multiforme  |  1
C0042769  |  viral infection  |  1
C0042769  |  viral disease  |  1
C0016085  |  filariasis  |  1
C0042769  |  viral infections  |  1
C0027765  |  neurological disorder  |  1
C0023281  |  leishmaniasis  |  1
C0042769  |  viral diseases  |  1
C0027819  |  neuroblastoma  |  1
C0027765  |  neurological disorders  |  1
Curated Gene(Waiting for update.)
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:98)
7920  |  ABHD16A  |  2.275  |  DISEASES
3267  |  AGFG1  |  3.06  |  DISEASES
10541  |  ANP32B  |  2.818  |  DISEASES
7917  |  BAG6  |  1.229  |  DISEASES
54828  |  BCAS3  |  3.45  |  DISEASES
815  |  CAMK2A  |  2.011  |  DISEASES
834  |  CASP1  |  1.392  |  DISEASES
57091  |  CASS4  |  2.154  |  DISEASES
81669  |  CCNL2  |  2.169  |  DISEASES
959  |  CD40LG  |  2.831  |  DISEASES
1103  |  CHAT  |  1.752  |  DISEASES
57019  |  CIAPIN1  |  2.14  |  DISEASES
51727  |  CMPK1  |  2.278  |  DISEASES
10675  |  CSPG5  |  1.811  |  DISEASES
1641  |  DCX  |  1.451  |  DISEASES
1791  |  DNTT  |  1.065  |  DISEASES
1859  |  DYRK1A  |  1.82  |  DISEASES
1915  |  EEF1A1  |  1.185  |  DISEASES
133584  |  EGFLAM  |  3.895  |  DISEASES
2035  |  EPB41  |  2.554  |  DISEASES
2060  |  EPS15  |  1.795  |  DISEASES
30816  |  ERVW-1  |  4.096  |  DISEASES
7430  |  EZR  |  1.423  |  DISEASES
356  |  FASLG  |  1.12  |  DISEASES
2242  |  FES  |  1.204  |  DISEASES
2314  |  FLII  |  1.312  |  DISEASES
2316  |  FLNA  |  2.069  |  DISEASES
2760  |  GM2A  |  1.82  |  DISEASES
2804  |  GOLGB1  |  1.204  |  DISEASES
7918  |  GPANK1  |  2.554  |  DISEASES
84706  |  GPT2  |  1.743  |  DISEASES
51454  |  GULP1  |  2.482  |  DISEASES
2996  |  GYPE  |  1.086  |  DISEASES
8091  |  HMGA2  |  1.195  |  DISEASES
84525  |  HOPX  |  1.476  |  DISEASES
3399  |  ID3  |  1.144  |  DISEASES
3418  |  IDH2  |  1.231  |  DISEASES
3433  |  IFIT2  |  2.828  |  DISEASES
8519  |  IFITM1  |  1.463  |  DISEASES
3441  |  IFNA4  |  2.88  |  DISEASES
3456  |  IFNB1  |  1.919  |  DISEASES
9641  |  IKBKE  |  1.774  |  DISEASES
3664  |  IRF6  |  1.299  |  DISEASES
9636  |  ISG15  |  1.017  |  DISEASES
3840  |  KPNA4  |  3.289  |  DISEASES
3916  |  LAMP1  |  1.448  |  DISEASES
126364  |  LRRC25  |  2.067  |  DISEASES
23764  |  MAFF  |  2.207  |  DISEASES
4099  |  MAG  |  1.448  |  DISEASES
23139  |  MAST2  |  1.15  |  DISEASES
4155  |  MBP  |  3.154  |  DISEASES
9968  |  MED12  |  2.092  |  DISEASES
79104  |  MEG8  |  3.859  |  DISEASES
4519  |  MT-CYB  |  1.548  |  DISEASES
4599  |  MX1  |  1.775  |  DISEASES
4734  |  NEDD4  |  2.188  |  DISEASES
11188  |  NISCH  |  1.138  |  DISEASES
58484  |  NLRC4  |  1.024  |  DISEASES
4881  |  NPR1  |  1.413  |  DISEASES
8021  |  NUP214  |  1.277  |  DISEASES
4938  |  OAS1  |  1.476  |  DISEASES
4948  |  OCA2  |  2.897  |  DISEASES
100506658  |  OCLN  |  1.069  |  DISEASES
4976  |  OPA1  |  2.258  |  DISEASES
5030  |  P2RY4  |  1.984  |  DISEASES
5077  |  PAX3  |  1.955  |  DISEASES
5256  |  PHKA2  |  1.682  |  DISEASES
55361  |  PI4K2A  |  2.067  |  DISEASES
139728  |  PNCK  |  1.325  |  DISEASES
5455  |  POU3F3  |  1.674  |  DISEASES
56980  |  PRDM10  |  1.5  |  DISEASES
10549  |  PRDX4  |  1.547  |  DISEASES
5664  |  PSEN2  |  2.316  |  DISEASES
5670  |  PSG2  |  2.88  |  DISEASES
57111  |  RAB25  |  1.769  |  DISEASES
23543  |  RBFOX2  |  1.95  |  DISEASES
343035  |  RD3  |  1.633  |  DISEASES
83695  |  RHNO1  |  1.189  |  DISEASES
6050  |  RNH1  |  2.145  |  DISEASES
404552  |  SCGB1D4  |  1.151  |  DISEASES
9728  |  SECISBP2L  |  2.071  |  DISEASES
5104  |  SERPINA5  |  2.678  |  DISEASES
1811  |  SLC26A3  |  1.925  |  DISEASES
94161  |  SNORD46  |  2.158  |  DISEASES
26793  |  SNORD56  |  4.055  |  DISEASES
6772  |  STAT1  |  1.55  |  DISEASES
26136  |  TES  |  2.195  |  DISEASES
51284  |  TLR7  |  1.174  |  DISEASES
340061  |  TMEM173  |  1.869  |  DISEASES
7124  |  TNF  |  1.764  |  DISEASES
8794  |  TNFRSF10C  |  1.088  |  DISEASES
121278  |  TPH2  |  1.565  |  DISEASES
51592  |  TRIM33  |  1.589  |  DISEASES
7318  |  UBA7  |  1.997  |  DISEASES
8725  |  URI1  |  1.685  |  DISEASES
6375  |  XCL1  |  1.221  |  DISEASES
7784  |  ZP3  |  1.786  |  DISEASES
57829  |  ZP4  |  2.263  |  DISEASES
Locus(Waiting for update.)
Disease ID 912
Disease rabies
Integrated Phenotype
HPO | Name(Total Integrated Phenotypes:19)
HP:0001250  |  Seizures
HP:0003401  |  Paresthesia
HP:0000708  |  Behavioral abnormality
HP:0001645  |  Sudden cardiac death
HP:0003781  |  Excessive salivation
HP:0002014  |  Diarrhea
HP:0100021  |  Cerebral palsy
HP:0001604  |  Vocal cord paresis
HP:0000738  |  Hallucinations
HP:0000716  |  Depression
HP:0002017  |  Nausea and vomiting
HP:0100785  |  Insomnia
HP:0001945  |  Fever
HP:0004372  |  Reduced consciousness/confusion
HP:0007018  |  Attention deficit hyperactivity disorder
HP:0002039  |  Anorexia
HP:0100776  |  Recurrent pharyngitis
HP:0002076  |  Migraine
HP:0000739  |  Anxiety
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:12)
HP:0003470  |  Inability to move  |  2
HP:0010783  |  Erythema  |  2
HP:0003287  |  Abnormality of mitochondrial metabolism  |  1
HP:0002719  |  infections, recurrent  |  1
HP:0001289  |  Confusion  |  1
HP:0003006  |  Neuroblastoma  |  1
HP:0001541  |  Ascites  |  1
HP:0000989  |  pruritis  |  1
HP:0010280  |  Stomatitis  |  1
HP:0000718  |  Aggressive behaviour  |  1
HP:0000708  |  Behavioral problems  |  1
HP:0000211  |  Trismus  |  1
Disease ID 912
Disease rabies
Manually Symptom
UMLS  | Name(Total Manually Symptoms:21)
C2711548  |  infectious process
C2364133  |  infection
C2127436  |  ascending paralysis
C1962971  |  myocarditis
C1518296  |  neuropathogenesis
C1264606  |  persistent infection
C0751378  |  neurologic signs
C0426359  |  urinary symptoms
C0277551  |  enzootic disease
C0262471  |  ent problem
C0235031  |  neurological symptoms
C0042749  |  viraemia
C0035222  |  acute respiratory distress syndrome
C0033117  |  priapism
C0032285  |  pneumonitis
C0022660  |  acute renal failure
C0021051  |  immunodeficiency
C0020453  |  hyperesthesia
C0014070  |  encephalomyelitis
C0014038  |  encephalitis
C0004936  |  mental disorders
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:3)
C0009450  |  infection  |  43
C0751378  |  neurologic signs  |  2
C0235031  |  neurological symptoms  |  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:4)
HP ID HP Name MP ID MP Name Annotation
HP:0007018Attention deficit hyperactivity disorderMP:0001399hyperactivitygeneral restlessness or excessive movement; more frequent movement from one place to another or having an increased state of activity
HP:0003781Excessive salivationMP:0000622increased salivationgreater than normal amounts of flowing saliva
HP:0002017Nausea and vomitingMP:0010426abnormal heart and great artery attachmentany anomaly in the in the position or pattern of the connection site of the heart to any of the great arteries, including the pulmonary artery and aorta
HP:0001645Sudden cardiac deathMP:0012557decreased calcium uptake by cardiac muscledecreased directed movement of calcium ions into cardiac muscle; decreased or disrupted uptake may give rise to energetic deficit and oxidative stress. leading to cardiac disease
Mapped by homologous gene(Total Items:19)
HP ID HP Name MP ID MP Name Annotation
HP:0100021Cerebral palsyMP:0013026decreased Ly6C low monocyte numberdecrease in the number of monocytes that express low levels of Ly6C and low MHC class II that represent a subset of patrolling monocytes
HP:0001945FeverMP:0020254decreased collagen leveldecreased level of the main structural protein of the various connective tissues in animals
HP:0000739AnxietyMP:0020329decreased capillary densityreduction in the number of capillaries in a given cross-sectional area of a tissue
HP:0000738HallucinationsMP:0020329decreased capillary densityreduction in the number of capillaries in a given cross-sectional area of a tissue
HP:0002076MigraineMP:0020329decreased capillary densityreduction in the number of capillaries in a given cross-sectional area of a tissue
HP:0000716DepressionMP:0020329decreased capillary densityreduction in the number of capillaries in a given cross-sectional area of a tissue
HP:0001250SeizuresMP:3000003abnormal Ebner's gland morphologyany structural anomaly of the serous salivary glands which reside adjacent to the moats surrounding the circumvallate and foliate papillae just anterior to the posterior third of the tongue, anterior to the terminal sulcus; these exocrine glands secrete l
HP:0004372Reduced consciousness/confusionMP:0013405increased circulating lactate levelgreater amount of lactate in the blood which is produced from pyruvate by lactate dehydrogenase
HP:0100776Recurrent pharyngitisMP:0013716hypolactationpartial failure, or reduced ability to produce or secrete milk from the mammary gland
HP:0000708Behavioral abnormalityMP:0020316decreased vascular endothelial cell proliferationdecrease in the expansion rate of any vascular endothelial cell population by cell division
HP:0001645Sudden cardiac deathMP:0020329decreased capillary densityreduction in the number of capillaries in a given cross-sectional area of a tissue
HP:0002014DiarrheaMP:0020220decreased tear productiondecreased production of the amount of fluid produced in the eye
HP:0003401ParesthesiaMP:0014185cerebellum atrophyacquired diminution of the size of the cerebellum associated with wasting as from death and reabsorption of cells, diminished cellular proliferation, decreased cellular volume, pressure, ischemia, malnutrition, reduced function or malfunction, or hormonal
HP:0100785InsomniaMP:0020187altered susceptibility to prion infectionaltered likelihood that an organism will develop ill effects from the small proteinaceous infectious particles which are resistant to inactivation by procedures that modify nucleic acids and which contain an abnormal isoform of a cellular protein that is
HP:0007018Attention deficit hyperactivity disorderMP:0020169increased thyroid gland weighthigher than average weight of the thyroid gland
HP:0002039AnorexiaMP:0020137decreased bone mineralizationdecrease in the rate at which minerals are deposited into bone
HP:0003781Excessive salivationMP:0012559decreased forebrain volumedecrease from the average range of forebrain volume compared to normal
HP:0001604Vocal cord paresisMP:0013438dysmyelinationreduced amount of myelin present in the form of a myelin sheath surrounding an axon due to defects in the synthesis and formation of myelin
HP:0002017Nausea and vomitingMP:0020220decreased tear productiondecreased production of the amount of fluid produced in the eye
Disease ID 912
Disease rabies
Case(Waiting for update.)