OMOP Concept 500000101
OMOP Angioedema 1
ClassificationConditionCohort500000101Cohort
Maps from
0
Descendants
41
Valid from
1 Jan 1970
Valid to
31 Dec 2099
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Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Narrower concepts
(41)Included automatically when you query with descendants.
- 1Angioedema
- 2Acquired angioedema type I
- 2Acquired angioedema type II
- 2Allergic angioedema
- 2Angioedema due to disorder of kinin metabolism
- 2Angioedema of eyelid
- 2Angioedema of lip
- 2Angioedema of tongue
- 2Autoimmune angioedema
- 2Azo-dye-induced angioedema-urticaria
- 2Chemical-aggravated angioedema-urticaria
- 2Cholinergic angioedema
- 2Drug-induced angioedema-urticaria
- 2Episodic angioedema with eosinophilia
- 2Exacerbation of angioedema
- 2Hereditary angioedema
- 2Idiopathic angioedema
- 2Physical angioedema
- 2Respiratory angioedema
- 2Sodium benzoate-induced angioedema-urticaria
- 3Acquired angioedema due to C1 inhibitor autoantibody
- 3Acquired C1 esterase inhibitor deficiency
- 3Allergic angioedema due to bite and/or sting
- 3Allergic angioedema due to ingested food
- 3Angioedema caused by angiotensin-converting-enzyme inhibitor
- 3Angioedema of gingiva due to deficiency of C1 esterase inhibitor
- 3Drug-aggravated angioedema-urticaria
- 3Food-induced angioedema-urticaria
- 3Hereditary angioedema with C1Inh (C1 esterase inhibitor) deficiency
- 3Hereditary angioedema with normal C1 esterase inhibitor activity
- 3Hereditary C1 esterase inhibitor deficiency - deficient factor
- 3Hereditary C1 esterase inhibitor deficiency - dysfunctional factor
- 3Hevea brasiliensis latex protein-induced angioedema-urticaria
- 3NSAID-induced angioedema-urticaria
- 3Penicillin-induced angioedema-urticaria
- 3Venom-induced angioedema-urticaria
- 3Vibratory angioedema
- 4ACE inhibitor-aggravated angioedema
- 4Acquired angioedema due to lymphoproliferative disorder
- 4Aspirin-induced angioedema-urticaria
- 4Intestinal angioedema caused by angiotensin-converting enzyme inhibitor
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