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Hereditary Angioedema Types I and II
Known as:
Deficiency of C1 Esterase Inhibitor
, Hereditary Angioedema Types I and II [Disease/Finding]
, C1 Esterase Inhibitor, Deficiency Of
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Autosomal dominant inherited disorders characterized by abnormalities of C1 inhibitor. Patients present with swelling of the skin, subcutaneous…
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National Institutes of Health
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Related topics
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10 relations
Angioedemas, Hereditary
C1 esterase inhibitor
In Blood
Microbiological
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Hereditary Angioedema Type I
Hereditary Angioedema Type II
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Association of hereditary angioedema type 1 with developmental anomalies due to a large and unusual de novo pericentromeric rearrangement of chromosome 11 spanning the entire C1 inhibitor gene…
D. Ebo
,
B. Blaumeiser
,
+6 authors
H. Poirel
Journal of Allergy and Clinical Immunology: In…
2019
Corpus ID: 53016096
Review
2006
Review
2006
[Hereditary angioedema. A report of a case and literature review].
N. J. Jiménez Saab
,
J. Gómez Vera
,
J. L. López Tiro
,
S. Nieto Martínez
,
C. P. Pliego Reyes
Revista Alergia México
2006
Corpus ID: 44277347
Hereditary angioedema is a congenital disorder with recurrent attacks of localized swelling of submucosal and subcutaneous tissue…
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