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	mumps

Disease ID	1540
Disease	mumps
Definition	An acute infectious disease caused by RUBULAVIRUS, spread by direct contact, airborne droplet nuclei, fomites contaminated by infectious saliva, and perhaps urine, and usually seen in children under the age of 15, although adults may also be affected. (From Dorland, 28th ed)
Synonym	epidemic parotiditis epidemic parotitides epidemic parotitis infectious parotitis mumps (disorder) mumps [disease/finding] mumps parotitis mumps parotitis (disorder) mumps, nos parotitides, epidemic parotitis - epidemic parotitis, epidemic
DOID	DOID:10264
UMLS	C0026780
MeSH	D009107
SNOMED-CT	SNOMEDCT_US_2016_09_01:36989005;SNOMEDCT_US_2016_09_01:240526004
Comorbidity	UMLS \| Disease \| Sentences' Count(Total Sentences:19) C0015469 \| facial paralysis \| 1 C0021359 \| infertile \| 1 C0043037 \| common warts \| 1 C0020255 \| hydrocephalus \| 1 C0003864 \| arthritis \| 1 C0022661 \| end-stage renal disease \| 1 C0014038 \| encephalitis \| 1 C0025290 \| aseptic meningitis \| 1 C0025007 \| measles \| 1 C0042769 \| viral infection \| 1 C0043395 \| yellow fever \| 1 C0025289 \| meningitis \| 1 C0026780 \| parotitis \| 1 C0042373 \| vascular disease \| 1 C0008049 \| varicella \| 1 C0025309 \| meningoencephalitis \| 1 C0022660 \| acute renal failure \| 1 C0015464 \| facial nerve palsy \| 1 C0007222 \| cardiovascular disease \| 1
Curated Gene	(Waiting for update.)
Inferring Gene	(Waiting for update.)
Text Mined Gene	Entrez_id \| Symbol \| Score \| Resource(Total Genes:75) 2 \| A2M \| 1.549 \| DISEASES 103 \| ADAR \| 1.697 \| DISEASES 10189 \| ALYREF \| 1.551 \| DISEASES 154810 \| AMOTL1 \| 2.576 \| DISEASES 276 \| AMY1A \| 1.47 \| DISEASES 277 \| AMY1B \| 1.47 \| DISEASES 278 \| AMY1C \| 1.47 \| DISEASES 60489 \| APOBEC3G \| 1.267 \| DISEASES 9776 \| ATG13 \| 2.063 \| DISEASES 8573 \| CASK \| 1.504 \| DISEASES 9560 \| CCL4L2 \| 1.043 \| DISEASES 930 \| CD19 \| 2.181 \| DISEASES 959 \| CD40LG \| 5.857 \| DISEASES 27159 \| CHIA \| 1.178 \| DISEASES 170482 \| CLEC4C \| 1.162 \| DISEASES 93978 \| CLEC6A \| 2.322 \| DISEASES 147906 \| DACT3 \| 1.756 \| DISEASES 1805 \| DPT \| 4.734 \| DISEASES 2029 \| ENSA \| 1.869 \| DISEASES 30816 \| ERVW-1 \| 2.359 \| DISEASES 2214 \| FCGR3A \| 2.178 \| DISEASES 160897 \| GPR180 \| 1.503 \| DISEASES 2987 \| GUK1 \| 1.815 \| DISEASES 3055 \| HCK \| 1.144 \| DISEASES 3106 \| HLA-B \| 2.227 \| DISEASES 3108 \| HLA-DMA \| 1.191 \| DISEASES 3109 \| HLA-DMB \| 2.042 \| DISEASES 3115 \| HLA-DPB1 \| 1.529 \| DISEASES 3117 \| HLA-DQA1 \| 1.084 \| DISEASES 3123 \| HLA-DRB1 \| 1.583 \| DISEASES 3127 \| HLA-DRB5 \| 2.538 \| DISEASES 3309 \| HSPA5 \| 1.15 \| DISEASES 10964 \| IFI44L \| 2.035 \| DISEASES 3440 \| IFNA2 \| 2.583 \| DISEASES 3586 \| IL10 \| 1.76 \| DISEASES 3594 \| IL12RB1 \| 2.001 \| DISEASES 7850 \| IL1R2 \| 1.262 \| DISEASES 3559 \| IL2RA \| 1.994 \| DISEASES 83943 \| IMMP2L \| 2.038 \| DISEASES 10989 \| IMMT \| 1.075 \| DISEASES 3916 \| LAMP1 \| 1.286 \| DISEASES 100885779 \| LINC-ROR \| 1.777 \| DISEASES 64327 \| LMBR1 \| 1.273 \| DISEASES 4155 \| MBP \| 2.272 \| DISEASES 9961 \| MVP \| 1.905 \| DISEASES 4600 \| MX2 \| 1.125 \| DISEASES 4938 \| OAS1 \| 1.314 \| DISEASES 4939 \| OAS2 \| 1.733 \| DISEASES 4942 \| OAT \| 1.944 \| DISEASES 103752588 \| PACERR \| 1.191 \| DISEASES 23556 \| PIGN \| 1.447 \| DISEASES 5478 \| PPIA \| 1.539 \| DISEASES 100169750 \| PRINS \| 1.799 \| DISEASES 8559 \| PRPF18 \| 3.106 \| DISEASES 5888 \| RAD51 \| 1.451 \| DISEASES 5649 \| RELN \| 1.508 \| DISEASES 6015 \| RING1 \| 1.421 \| DISEASES 3921 \| RPSA \| 1.227 \| DISEASES 91543 \| RSAD2 \| 1.699 \| DISEASES 6288 \| SAA1 \| 1.048 \| DISEASES 404552 \| SCGB1D4 \| 1.079 \| DISEASES 23451 \| SF3B1 \| 2.037 \| DISEASES 140885 \| SIRPA \| 1.913 \| DISEASES 55315 \| SLC29A3 \| 1.038 \| DISEASES 26768 \| SNORA73B \| 2.256 \| DISEASES 8651 \| SOCS1 \| 1.624 \| DISEASES 375686 \| SPATC1 \| 3.796 \| DISEASES 79925 \| SPEF2 \| 2.678 \| DISEASES 6772 \| STAT1 \| 1.142 \| DISEASES 6942 \| TCF20 \| 1.493 \| DISEASES 7018 \| TF \| 1.627 \| DISEASES 284486 \| THEM5 \| 1.475 \| DISEASES 7124 \| TNF \| 1.558 \| DISEASES 8718 \| TNFRSF25 \| 3.452 \| DISEASES 7272 \| TTK \| 1.22 \| DISEASES
Locus	(Waiting for update.)

Disease ID	1540
Disease	mumps
Integrated Phenotype	(Waiting for update.)
Text Mined Phenotype	HPO \| Name \| Sentences' Count(Total Phenotypes:21) HP:0100796 \| Orchitis \| 2 HP:0011450 \| CNS infection \| 1 HP:0001919 \| Acute renal failure \| 1 HP:0001336 \| Myoclonic jerks \| 1 HP:0003470 \| Inability to move \| 1 HP:0001300 \| Parkinsonism \| 1 HP:0200043 \| Verrucae \| 1 HP:0012027 \| Laryngeal edema \| 1 HP:0001287 \| Meningitis \| 1 HP:0003774 \| End-stage renal failure \| 1 HP:0001751 \| Vestibular dysfunction \| 1 HP:0001250 \| Seizures \| 1 HP:0002304 \| Akinesia \| 1 HP:0010543 \| Opsoclonus \| 1 HP:0001369 \| Arthritis \| 1 HP:0002383 \| Encephalitis \| 1 HP:0010628 \| Facial palsy, unilateral or bilateral \| 1 HP:0000969 \| Dropsy \| 1 HP:0000238 \| Nonsyndromal hydrocephalus \| 1 HP:0007209 \| Facial paresis \| 1 HP:0011850 \| Parotitis \| 1

Disease ID	1540
Disease	mumps
Manually Symptom	UMLS \| Name(Total Manually Symptoms:63) C2364133 \| infection C2363781 \| multiple cerebral infarction C2203646 \| jaundice C2096293 \| vertigo C2029884 \| hearing loss C2004072 \| acute aseptic meningitis C1963198 \| pancreatitis C1962986 \| glaucoma C1384666 \| hearing impairment C1299910 \| kerato-uveitis C1278797 \| postnatal infection C1148477 \| sudden deafness C1135207 \| ataxia C0936254 \| polyradiculoneuritis C0857305 \| thrombocytopenic purpura C0852283 \| neonatal respiratory distress C0581883 \| total deafness C0581883 \| deafness C0581883 \| complete deafness C0581883 \| bilateral deafness C0398650 \| immune thrombocytopenic purpura C0342176 \| giant cell thyroiditis C0277792 \| pathognomonic sign C0270627 \| acute transverse myelitis C0242567 \| opsoclonus C0235238 \| paralysis of accommodation C0231528 \| myalgia C0178879 \| obstructive uropathy C0155550 \| neural hearing loss C0155301 \| retrobulbar neuritis C0154874 \| neuroretinitis C0086543 \| cataracts C0043117 \| idiopathic thrombocytopenic purpura C0042749 \| viremia C0039070 \| fainting C0035435 \| rheumatism C0032285 \| pneumonia C0029191 \| orchitis C0029051 \| oophoritis C0027765 \| nervous system disorders C0027697 \| nephritis C0025309 \| meningoencephalitis C0025297 \| viral meningitis C0025290 \| aseptic meningitis C0025289 \| meningitis C0024266 \| lymphocytic meningitis C0022893 \| labyrinthitis C0022890 \| labyrinthine disorder C0022658 \| nephropathy C0022568 \| keratitis C0021051 \| immunodeficiency C0020619 \| hypogonadism C0018784 \| sensorineural hearing loss C0015230 \| rash C0014534 \| epididymitis C0014070 \| encephalomyelitis C0014038 \| encephalitis C0013604 \| oedema C0007813 \| cerebrospinal meningitis C0007758 \| cerebellar ataxia C0003864 \| arthritis C0002878 \| haemolytic anaemia C0001339 \| acute pancreatitis
Text Mined Symptom	UMLS \| Name \| Sentences' Count(Total Symptoms:10) C0009450 \| infection \| 5 C0029191 \| orchitis \| 2 C0003864 \| arthritis \| 1 C0013604 \| oedema \| 1 C0242567 \| opsoclonus \| 1 C0025290 \| aseptic meningitis \| 1 C1384666 \| hearing loss \| 1 C0025289 \| meningitis \| 1 C0014038 \| encephalitis \| 1 C0025309 \| meningoencephalitis \| 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	1540
Disease	mumps
Case	(Waiting for update.)

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