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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine



   yellow fever
  

Disease ID 966
Disease yellow fever
Definition
An acute infectious disease primarily of the tropics, caused by a virus and transmitted to man by mosquitoes of the genera Aedes and Haemagogus. The severe form is characterized by fever, HEMOLYTIC JAUNDICE, and renal damage.
Synonym
[x]yellow fever, unspecified
[x]yellow fever, unspecified (disorder)
fever, yellow
fevers, yellow
yellow fever (disorder)
yellow fever [disease/finding]
yellow fever nos
yellow fever unspecified
yellow fever unspecified (disorder)
yellow fever virus infection
yellow fever, nos
yellow fever, unspecified
yellow fevers
yf - yellow fever
Orphanet
DOID
ICD10
UMLS
C0043395
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:6)
C0025007  |  measles  |  3
C0024530  |  malaria  |  2
C0026780  |  mumps  |  1
C0035920  |  rubella  |  1
C0559469  |  egg allergy  |  1
C0023364  |  leptospirosis  |  1
Curated Gene(Waiting for update.)
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:76)
2  |  A2M  |  1.362  |  DISEASES
10195  |  ALG3  |  2.494  |  DISEASES
250  |  ALPP  |  2.669  |  DISEASES
64115  |  C10orf54  |  3.095  |  DISEASES
755  |  C21orf2  |  4.516  |  DISEASES
22900  |  CARD8  |  1.83  |  DISEASES
79872  |  CBLL1  |  2.769  |  DISEASES
388372  |  CCL4L1  |  1.427  |  DISEASES
9560  |  CCL4L2  |  1.281  |  DISEASES
959  |  CD40LG  |  4.497  |  DISEASES
170482  |  CLEC4C  |  1.4  |  DISEASES
10675  |  CSPG5  |  3.435  |  DISEASES
4283  |  CXCL9  |  1.175  |  DISEASES
192668  |  CYS1  |  1.65  |  DISEASES
147906  |  DACT3  |  2.083  |  DISEASES
51428  |  DDX41  |  1.298  |  DISEASES
23586  |  DDX58  |  2.189  |  DISEASES
23405  |  DICER1  |  1.455  |  DISEASES
1805  |  DPT  |  3.383  |  DISEASES
29102  |  DROSHA  |  2.131  |  DISEASES
83658  |  DYNLRB1  |  1.79  |  DISEASES
6993  |  DYNLT1  |  1.464  |  DISEASES
51386  |  EIF3L  |  3.809  |  DISEASES
1999  |  ELF3  |  2.478  |  DISEASES
30816  |  ERVW-1  |  4.146  |  DISEASES
2114  |  ETS2  |  1.117  |  DISEASES
2213  |  FCGR2B  |  1.626  |  DISEASES
2214  |  FCGR3A  |  1.353  |  DISEASES
51218  |  GLRX5  |  2.197  |  DISEASES
2813  |  GP2  |  1.379  |  DISEASES
3062  |  HCRTR2  |  2.431  |  DISEASES
5654  |  HTRA1  |  1.129  |  DISEASES
3586  |  IL10  |  1.733  |  DISEASES
51135  |  IRAK4  |  1.402  |  DISEASES
3665  |  IRF7  |  2.011  |  DISEASES
9636  |  ISG15  |  1.182  |  DISEASES
23210  |  JMJD6  |  1.281  |  DISEASES
3916  |  LAMP1  |  1.568  |  DISEASES
389421  |  LIN28B  |  1.407  |  DISEASES
497634  |  LINC00293  |  4.114  |  DISEASES
100885779  |  LINC-ROR  |  1.102  |  DISEASES
116511  |  MAS1L  |  2.672  |  DISEASES
284424  |  MIR7-3HG  |  1.817  |  DISEASES
4512  |  MT-CO1  |  2.727  |  DISEASES
4513  |  MT-CO2  |  1.242  |  DISEASES
4538  |  MT-ND4  |  1.954  |  DISEASES
4540  |  MT-ND5  |  1.248  |  DISEASES
4615  |  MYD88  |  1.016  |  DISEASES
23218  |  NBEAL2  |  1.437  |  DISEASES
4700  |  NDUFA6  |  2.079  |  DISEASES
246734  |  NPCDR1  |  1.128  |  DISEASES
4923  |  NTSR1  |  1.025  |  DISEASES
4938  |  OAS1  |  1.641  |  DISEASES
4939  |  OAS2  |  3.017  |  DISEASES
8398  |  PLA2G6  |  1.103  |  DISEASES
5454  |  POU3F2  |  1.65  |  DISEASES
5478  |  PPIA  |  2.457  |  DISEASES
149830  |  PRNT  |  5.597  |  DISEASES
5625  |  PRODH  |  1.378  |  DISEASES
6050  |  RNH1  |  1.353  |  DISEASES
6161  |  RPL32  |  2.307  |  DISEASES
6175  |  RPLP0  |  1.864  |  DISEASES
6176  |  RPLP1  |  2.819  |  DISEASES
6181  |  RPLP2  |  1.849  |  DISEASES
6235  |  RPS29  |  2.727  |  DISEASES
23212  |  RRS1  |  1.139  |  DISEASES
91543  |  RSAD2  |  2.027  |  DISEASES
123228  |  SENP8  |  5.832  |  DISEASES
6614  |  SIGLEC1  |  1.612  |  DISEASES
11005  |  SPINK5  |  1.175  |  DISEASES
6996  |  TDG  |  1.722  |  DISEASES
51284  |  TLR7  |  2.56  |  DISEASES
54106  |  TLR9  |  2.311  |  DISEASES
7124  |  TNF  |  2.282  |  DISEASES
8718  |  TNFRSF25  |  1.407  |  DISEASES
11169  |  WDHD1  |  2.048  |  DISEASES
Locus(Waiting for update.)
Disease ID 966
Disease yellow fever
Integrated Phenotype
HPO | Name(Total Integrated Phenotypes:29)
HP:0002239  |  Gastrointestinal hemorrhage
HP:0002027  |  Abdominal pain
HP:0400008  |  Menometrorrhagia
HP:0001287  |  Meningitis
HP:0002383  |  Encephalitis
HP:0000093  |  Proteinuria
HP:0000083  |  Renal insufficiency
HP:0001635  |  Congestive heart failure
HP:0002829  |  Arthralgia
HP:0006554  |  Acute hepatic failure
HP:0003326  |  Myalgia
HP:0001254  |  Lethargy
HP:0002014  |  Diarrhea
HP:0100520  |  Oliguria
HP:0002615  |  Hypotension
HP:0000112  |  Nephropathy
HP:0002017  |  Nausea and vomiting
HP:0001944  |  Dehydration
HP:0000952  |  Jaundice
HP:0005268  |  Spontaneous abortion
HP:0011675  |  Arrhythmia
HP:0001945  |  Fever
HP:0002045  |  Hypothermia
HP:0000613  |  Photophobia
HP:0100749  |  Chest pain
HP:0006543  |  Cardiorespiratory arrest
HP:0002039  |  Anorexia
HP:0002315  |  Headache
HP:0002047  |  Malignant hyperthermia
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:1)
HP:0000952  |  Yellow skin  |  1
Disease ID 966
Disease yellow fever
Manually Symptom
UMLS  | Name(Total Manually Symptoms:2)
C1963178  |  myelitis
C0019104  |  haemorrhagic fever
Text Mined Symptom(Waiting for update.)
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:6)
HP ID HP Name MP ID MP Name Annotation
HP:0002239Gastrointestinal hemorrhageMP:0012305umbilical cord hemorrhagebleeding into or from the umbilical cord
HP:0006554Acute hepatic failureMP:0002628hepatic steatosisan accumulation of fat deposits in the liver
HP:0000083Renal insufficiencyMP:0003335exocrine pancreatic insufficiencyinadequate synthesis and/or secretion of digestive enzymes by the exocrine portion of the pancreas, usually due to loss of acinar tissue from idiopathic atrophy or acute or chronic inflammation, causing maldigestion and malabsorption of nutrients
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:0002047Malignant hyperthermiaMP:0020214susceptible to malignant hyperthermiaincreased susceptibility to hyperthermia triggered by exposure to certain drugs used for general anesthesia, specifically the volatile anesthetic agents and the neuromuscular blocking agent, succinylcholine
HP:0001635Congestive heart failureMP:0011925abnormal heart echocardiography featureany anomaly in echocardiographic representation of systolic and diastolic function, ventricular compliance, valvular function, or interventricular septum features
Mapped by homologous gene(Total Items:27)
HP ID HP Name MP ID MP Name Annotation
HP:0001945FeverMP:0020254decreased collagen leveldecreased level of the main structural protein of the various connective tissues in animals
HP:0006554Acute hepatic failureMP:0020137decreased bone mineralizationdecrease in the rate at which minerals are deposited into bone
HP:0011675ArrhythmiaMP:0020309increased creatine kinase activityincreased ability of to catalyze the reaction: ATP + creatine = N-phosphocreatine + ADP + 2 H(+).
HP:0001944DehydrationMP:0014206decreased intestinal epithelial sodium ion transmembrane transport
HP:0002315HeadacheMP:0020137decreased bone mineralizationdecrease in the rate at which minerals are deposited into bone
HP:0000112NephropathyMP:0020234decreased basal metabolismdecrease in heat production of an organism at the lowest level of cell chemistry in an inactive, awake, and fasting state
HP:0001287MeningitisMP:0020215impaired blood coagulationimpaired ability of the blood to clot
HP:0000093ProteinuriaMP:0020216decreased circulating complement protein levelless than normal levels of the serum proteins that act sequentially to allow for the direct killing of microbes, the disposal of immune complexes, and the regulation of other immune processes
HP:0002239Gastrointestinal hemorrhageMP:0020215impaired blood coagulationimpaired ability of the blood to clot
HP:0002014DiarrheaMP:0020220decreased tear productiondecreased production of the amount of fluid produced in the eye
HP:0002017Nausea and vomitingMP:0020220decreased tear productiondecreased production of the amount of fluid produced in the eye
HP:0002039AnorexiaMP:0020137decreased bone mineralizationdecrease in the rate at which minerals are deposited into bone
HP:0000952JaundiceMP:0020215impaired blood coagulationimpaired ability of the blood to clot
HP:0002383EncephalitisMP:0020215impaired blood coagulationimpaired ability of the blood to clot
HP:0002829ArthralgiaMP:0020154impaired humoral immune responseimpaired response of the immune system that mediates secreted antibodies produced in B cells
HP:0002045HypothermiaMP:0020137decreased bone mineralizationdecrease in the rate at which minerals are deposited into bone
HP:0000083Renal insufficiencyMP:0020316decreased vascular endothelial cell proliferationdecrease in the expansion rate of any vascular endothelial cell population by cell division
HP:0002027Abdominal painMP:0020220decreased tear productiondecreased production of the amount of fluid produced in the eye
HP:0001254LethargyMP:0020137decreased bone mineralizationdecrease in the rate at which minerals are deposited into bone
HP:0003326MyalgiaMP:0020309increased creatine kinase activityincreased ability of to catalyze the reaction: ATP + creatine = N-phosphocreatine + ADP + 2 H(+).
HP:0001635Congestive heart failureMP:0020329decreased capillary densityreduction in the number of capillaries in a given cross-sectional area of a tissue
HP:0000613PhotophobiaMP:0020220decreased tear productiondecreased production of the amount of fluid produced in the eye
HP:0100749Chest painMP:0020154impaired humoral immune responseimpaired response of the immune system that mediates secreted antibodies produced in B cells
HP:0002615HypotensionMP:0020214susceptible to malignant hyperthermiaincreased susceptibility to hyperthermia triggered by exposure to certain drugs used for general anesthesia, specifically the volatile anesthetic agents and the neuromuscular blocking agent, succinylcholine
HP:0006543Cardiorespiratory arrestMP:0011100preweaning lethality, complete penetrancedeath of all organisms of a given genotype in a population between fertilization and weaning age (Mus: approximately 3-4 weeks of age)
HP:0002047Malignant hyperthermiaMP:0020214susceptible to malignant hyperthermiaincreased susceptibility to hyperthermia triggered by exposure to certain drugs used for general anesthesia, specifically the volatile anesthetic agents and the neuromuscular blocking agent, succinylcholine
HP:0005268Spontaneous abortionMP:0020040decreased bone ossificationdecrease in the formation of bone or of a bony substance, or the conversion of fibrous tissue or of cartilage into bone or a bony substance
Disease ID 966
Disease yellow fever
Case(Waiting for update.)