hereditary angioedema

GPTKB entity

Statements (51)
Predicate Object
gptkbp:instanceOf genetic disorder
gptkbp:advertising educational campaigns
patient advocacy organizations
National Angioedema Awareness Day
gptkbp:associatedWith C1 inhibitor gene mutations
gptkbp:causedBy C1 inhibitor deficiency
gptkbp:clinicalTrials C1 inhibitor therapy
bradykinin receptor antagonists
newer therapies
gptkbp:community_service C1 inhibitor levels
C4 levels
gptkbp:demographics 1 in 50,000 to 1 in 150,000
gptkbp:diseaseResistance genetic testing
clinical evaluation
chronic condition
variable severity
can be managed with treatment
gptkbp:emergencyServices oxygen therapy
epinephrine
intubation if necessary
gptkbp:geneticDiversity 11q12.2
gptkbp:hasCapacity educational resources
medical professionals
support groups
gptkbp:hasService history of recurrent angioedema
low C1 inhibitor levels
low_C4_levels
https://www.w3.org/2000/01/rdf-schema#label hereditary angioedema
gptkbp:impact both genders
antifibrinolytics
C1 inhibitor replacement therapy
bradykinin receptor antagonists
gptkbp:inheritsFrom childhood or adolescence
gptkbp:introduced by_William_Osler
gptkbp:manager avoidance of triggers
gptkbp:nobleFamily autosomal dominant
gptkbp:relatedPatent asphyxiation
acquired angioedema
gastrointestinal obstruction
gptkbp:research ongoing studies on new therapies
gptkbp:riskManagement stress
trauma
hormonal changes
surgery
family history
gptkbp:symptoms abdominal pain
swelling
difficulty breathing
skin rash
gptkbp:type Type I
Type II