|
1 / 1
|
DeCS
|
|
 |
|
Descriptor English:
|
|
Hereditary Complement Deficiency Diseases
|
|
Descriptor Spanish:
|
|
Enfermedades por Deficiencia de Complemento Hereditario
|
|
Descriptor Portuguese:
|
|
Doenças da Deficiência Hereditária de Complemento
|
|
Synonyms English:
|
|
Complement Deficiencies
Complement Deficiency
Inherited Complement Deficiency Diseases
|
|
Tree Number:
|
|
C16.320.798.500
C20.673.795.500
|
|
Definition English:
|
|
Genetic disorders due to mutations in genes involved in COMPLEMENT SYSTEM PROTEINS. They are often classified into distinct pathway of complement activation where causative mutations are found (e.g., classical pathway, lectin pathway, alternative pathway, and terminal complement pathway). |
|
History Note English:
|
|
2020
|
|
Allowable Qualifiers English:
|
|
|
|
Record Number:
|
|
59119
|
|
Unique Identifier:
|
|
D000081208
|
Occurrence in VHL:
|
|
|
Similar:
|
|
DeCS
|