rabies |
Disease ID | 912 |
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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 |
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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 |
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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) |
Manually Genotype(Total Text Mining Genotypes:0) |
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(Waiting for update.) |
Text Mining Genotype(Total Genotypes:0) | |
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(Waiting for update.) |
All Snps(Total Genotypes:0) | |
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(Waiting for update.) |
GWASdb Annotation(Total Genotypes:0) | |
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(Waiting for update.) |
GWASdb Snp Trait(Total Genotypes:0) | |
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(Waiting for update.) |
Mapped by lexical matching(Total Items:4) | ||||
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HP ID | HP Name | MP ID | MP Name | Annotation |
HP:0007018 | Attention deficit hyperactivity disorder | MP:0001399 | hyperactivity | general restlessness or excessive movement; more frequent movement from one place to another or having an increased state of activity |
HP:0003781 | Excessive salivation | MP:0000622 | increased salivation | greater than normal amounts of flowing saliva |
HP:0002017 | Nausea and vomiting | MP:0010426 | abnormal heart and great artery attachment | any 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:0001645 | Sudden cardiac death | MP:0012557 | decreased calcium uptake by cardiac muscle | decreased 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) | ||||
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HP ID | HP Name | MP ID | MP Name | Annotation |
HP:0100021 | Cerebral palsy | MP:0013026 | decreased Ly6C low monocyte number | decrease in the number of monocytes that express low levels of Ly6C and low MHC class II that represent a subset of patrolling monocytes |
HP:0001945 | Fever | MP:0020254 | decreased collagen level | decreased level of the main structural protein of the various connective tissues in animals |
HP:0000739 | Anxiety | MP:0020329 | decreased capillary density | reduction in the number of capillaries in a given cross-sectional area of a tissue |
HP:0000738 | Hallucinations | MP:0020329 | decreased capillary density | reduction in the number of capillaries in a given cross-sectional area of a tissue |
HP:0002076 | Migraine | MP:0020329 | decreased capillary density | reduction in the number of capillaries in a given cross-sectional area of a tissue |
HP:0000716 | Depression | MP:0020329 | decreased capillary density | reduction in the number of capillaries in a given cross-sectional area of a tissue |
HP:0001250 | Seizures | MP:3000003 | abnormal Ebner's gland morphology | any 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:0004372 | Reduced consciousness/confusion | MP:0013405 | increased circulating lactate level | greater amount of lactate in the blood which is produced from pyruvate by lactate dehydrogenase |
HP:0100776 | Recurrent pharyngitis | MP:0013716 | hypolactation | partial failure, or reduced ability to produce or secrete milk from the mammary gland |
HP:0000708 | Behavioral abnormality | MP:0020316 | decreased vascular endothelial cell proliferation | decrease in the expansion rate of any vascular endothelial cell population by cell division |
HP:0001645 | Sudden cardiac death | MP:0020329 | decreased capillary density | reduction in the number of capillaries in a given cross-sectional area of a tissue |
HP:0002014 | Diarrhea | MP:0020220 | decreased tear production | decreased production of the amount of fluid produced in the eye |
HP:0003401 | Paresthesia | MP:0014185 | cerebellum atrophy | acquired 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:0100785 | Insomnia | MP:0020187 | altered susceptibility to prion infection | altered 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:0007018 | Attention deficit hyperactivity disorder | MP:0020169 | increased thyroid gland weight | higher than average weight of the thyroid gland |
HP:0002039 | Anorexia | MP:0020137 | decreased bone mineralization | decrease in the rate at which minerals are deposited into bone |
HP:0003781 | Excessive salivation | MP:0012559 | decreased forebrain volume | decrease from the average range of forebrain volume compared to normal |
HP:0001604 | Vocal cord paresis | MP:0013438 | dysmyelination | reduced 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:0002017 | Nausea and vomiting | MP:0020220 | decreased tear production | decreased production of the amount of fluid produced in the eye |
Disease ID | 912 |
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Disease | rabies |
Case | (Waiting for update.) |