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encyclopedia of Rare Disease Annotation for Precision Medicine

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	anaphylaxis

Disease ID	1200
Disease	anaphylaxis
Definition	An acute hypersensitivity reaction due to exposure to a previously encountered ANTIGEN. The reaction may include rapidly progressing URTICARIA, respiratory distress, vascular collapse, systemic SHOCK, and death.
Synonym	allergic shock anaphylactic reaction anaphylactic reactions anaphylactic shock anaphylaxis (disorder) anaphylaxis [disease/finding] anaphylaxis, generalized generalised anaphylaxis generalized anaphylaxis generalized anaphylaxis (disorder) obsolete anaphylaxis reaction, anaphylactic reactions, anaphylactic shock, anaphylactic systemic anaphylaxis systemic anaphylaxis (disorder)
UMLS	C0002792
MeSH	D000707
SNOMED-CT	SNOMEDCT_US_2016_09_01:39579001
Comorbidity	UMLS \| Disease \| Sentences' Count(Total Sentences:52) C0024899 \| mastocytosis \| 8 C0016470 \| food allergy \| 6 C0042109 \| urticaria \| 5 C0004096 \| asthma \| 5 C0577620 \| nut allergy \| 5 C0221013 \| systemic mastocytosis \| 5 C0085278 \| antiphospholipid syndrome \| 3 C0013502 \| hydatid cyst \| 3 C0015230 \| rash \| 3 C0024899 \| mast cell disease \| 2 C0079840 \| milk allergy \| 2 C1145670 \| respiratory failure \| 2 C0559469 \| egg allergy \| 2 C0155877 \| allergic asthma \| 2 C0024623 \| gastric cancer \| 1 C0035078 \| renal failure \| 1 C0016053 \| fibromyalgia \| 1 C0022660 \| acute kidney failure \| 1 C0018801 \| cardiac failure \| 1 C0014544 \| epilepsy \| 1 C1136033 \| cutaneous mastocytosis \| 1 C0013502 \| hydatidosis \| 1 C0018799 \| cardiac disease \| 1 C0016053 \| fibromyalgia syndrome \| 1 C0026986 \| myelodysplastic syndrome \| 1 C0032001 \| pituitary apoplexy \| 1 C0013595 \| eczema \| 1 C0034063 \| pulmonary edema \| 1 C0013182 \| drug allergy \| 1 C0007682 \| central nervous system disease \| 1 C0016470 \| food allergies \| 1 C0035078 \| kidney failure \| 1 C0010068 \| coronary disease \| 1 C0022660 \| acute renal failure \| 1 C0027765 \| nervous system disease \| 1 C0003467 \| anxiety \| 1 C0027765 \| nervous system diseases \| 1 C0006017 \| pertussis \| 1 C0022116 \| ischaemia \| 1 C0008311 \| cholangitis \| 1 C1565489 \| renal insufficiency \| 1 C0027051 \| myocardial infarction \| 1 C0027051 \| myocardial infarct \| 1 C0011991 \| diarrhea \| 1 C0040921 \| trichomoniasis \| 1 C1096063 \| intractable epilepsy \| 1 C0016470 \| food hypersensitivity \| 1 C0013502 \| hydatid disease \| 1 C0015230 \| exanthema \| 1 C0038218 \| status asthmaticus \| 1 C0007682 \| central nervous system diseases \| 1 C0030824 \| penicillin allergy \| 1
Curated Gene	Entrez_id \| Symbol \| Resource(Total Genes:4) 3827 \| KNG1 \| CTD_human 114548 \| NLRP3 \| CTD_human 374569 \| ASPG \| CTD_human 1241 \| LTB4R \| CTD_human
Inferring Gene	Entrez_id \| Symbol \| Resource(Total Genes:5) 183 \| AGT \| CIPHER 3827 \| KNG1 \| CTD_human 114548 \| NLRP3 \| CTD_human 1241 \| LTB4R \| CTD_human 374569 \| ASPG \| CTD_human
Text Mined Gene	(Waiting for update.)
Locus	(Waiting for update.)

Disease ID	1200
Disease	anaphylaxis
Integrated Phenotype	(Waiting for update.)
Text Mined Phenotype	HPO \| Name \| Sentences' Count(Total Phenotypes:52) HP:0012393 \| Allergy \| 24 HP:0002615 \| Low blood pressure \| 17 HP:0100495 \| Mastocytosis \| 9 HP:0000969 \| Dropsy \| 8 HP:0100665 \| Angiooedema \| 7 HP:0001025 \| Hives \| 6 HP:0002099 \| Asthma \| 6 HP:0001695 \| Cardiac arrest \| 6 HP:0002094 \| Dyspnea \| 3 HP:0001649 \| Tachycardia \| 3 HP:0001279 \| Syncope \| 2 HP:0012027 \| Laryngeal edema \| 2 HP:0000083 \| Renal insufficiency \| 2 HP:0100327 \| Cow milk allergy \| 2 HP:0002878 \| Respiratory failure \| 2 HP:0000988 \| Exanthem \| 2 HP:0001919 \| Acute renal failure \| 2 HP:0001677 \| Coronary artery disease \| 1 HP:0002242 \| Enteropathy \| 1 HP:0100845 \| Anaphylactic shock \| 1 HP:0011855 \| Pharyngeal edema \| 1 HP:0002014 \| Diarrhea \| 1 HP:0030149 \| Cardiovascular shock \| 1 HP:0004934 \| Vascular calcification \| 1 HP:0200151 \| Cutaneous mastocytosis \| 1 HP:0012531 \| Pain \| 1 HP:0001662 \| Bradycardia \| 1 HP:0012653 \| Acute severe asthma \| 1 HP:0001658 \| Myocardial infarction \| 1 HP:0001681 \| Angina pectoris \| 1 HP:0001941 \| acidemia \| 1 HP:0002013 \| Emesis \| 1 HP:0000989 \| pruritis \| 1 HP:0005943 \| Respiratory arrest \| 1 HP:0002475 \| Myelomeningocele \| 1 HP:0000739 \| Anxiety \| 1 HP:0002835 \| Aspiration \| 1 HP:0001945 \| Fever \| 1 HP:0040236 \| Hyperfibrinolysis \| 1 HP:0011106 \| Depleted blood volume \| 1 HP:0001297 \| Cerebral vascular events \| 1 HP:0007185 \| Loss of consciousness \| 1 HP:0100598 \| Pulmonary oedema \| 1 HP:0006543 \| Cardiorespiratory arrest \| 1 HP:0012418 \| Low blood oxygen level \| 1 HP:0001635 \| Congestive heart failure \| 1 HP:0002863 \| Myelodysplastic syndrome \| 1 HP:0010783 \| Erythema \| 1 HP:0000964 \| Eczema \| 1 HP:0012126 \| Gastric cancer \| 1 HP:0004756 \| Ventricular tachycardia \| 1 HP:0030151 \| Cholangitis \| 1

Disease ID	1200
Disease	anaphylaxis
Manually Symptom	UMLS \| Name(Total Manually Symptoms:19) C2598155 \| pain C2364072 \| depression C2039684 \| systemic symptoms C1555754 \| cardiovascular disease C1393529 \| vascular complications C0948268 \| hemodynamic instability C0422833 \| ent symptoms C0272285 \| heparin-induced thrombocytopenia C0264490 \| acute respiratory failure C0232197 \| fibrillation C0040034 \| thrombocytopenia C0034063 \| pulmonary edema C0032285 \| pulmonary inflammation C0020649 \| hypotension C0020456 \| hyperglycemia C0017178 \| gastrointestinal disorders C0012739 \| defibrination syndrome C0006266 \| bronchospasm C0001883 \| airway obstruction
Text Mined Symptom	UMLS \| Name \| Sentences' Count(Total Symptoms:4) C0020649 \| hypotension \| 11 C0006266 \| bronchospasm \| 2 C0948268 \| hemodynamic instability \| 1 C0030193 \| pain \| 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	1200
Disease	anaphylaxis
Case	(Waiting for update.)

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