hereditary angioedema types I and II

Preferred Label : hereditary angioedema types I and II;

MeSH definition : Forms of hereditary angioedema that occur due to mutations in the gene for COMPLEMENT C1 INHIBITOR PROTEIN. Type I hereditary angioedema is associated with reduced serum levels of complement C1 inhibitor protein. Type II hereditary angioedema is associated with the production of a non-functional complement C1 inhibitor protein.;

MeSH synonym : Angioedema, Hereditary, Types I and II; deficiency of C1 esterase inhibitor; C1 esterase inhibitor, deficiency of; hereditary angioedema type 1;

MeSH hyponym : hereditary angioedema type I; hereditary angioedema type II; Angioedema, Hereditary, Type I; Angioedema, Hereditary, Type II;

Details

Origin ID

D056829;

UMLS CUI

C2717905;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- Angioedema, hereditary, 1 [OMIM Phenotype]
- C1 esterase inhibitor deficiency [MedDRA LLT]
- Hereditary angioedema [MedDRA Preferred Term]
- Hereditary angioedema (disorder) [SNOMED CT concept]
- Hereditary angioedema type 1 [ORDO Disease]
- Hereditary angioedema type 2 [ORDO Disease]
- Hereditary angioedema type I [MedDRA LLT]
- Hereditary angioedema type II [MedDRA LLT]
- hereditary angioedema type I [DO Concept]
Currated CISMeF NLP mapping
- Hereditary Angioedema Types I and II [NCIt concept]
MeSH Descriptor(s) used for indexing
- complement C1 inhibitor protein [MeSH Descriptor]
Record concept(s)
- hereditary angioedema type I [MeSH concept]
- hereditary angioedema type II [MeSH concept]
- hereditary angioedema types I and II [MeSH concept]
See also
- complement C1 inhibitor protein [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hereditary Angioedema Types I and II [NCIt concept]
Validated automatic mappings to BTNT
- Hereditary C1 esterase inhibitor deficiency - deficient factor (disorder) [SNOMED CT concept]
- Hereditary angioedema type I [ICD-11 More detail]
- Hereditary angioedema type II [ICD-11 More detail]
- hereditary angioedema type I [Disease (Nov.)]
- hereditary angioedema type II [Disease (Nov.)]
Validated automatic mappings to NTBT
- hereditary angioedema [Disease (Nov.)]

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