Hereditary Complement Deficiency Diseases

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).

Year introduced: 2020

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Tree Number(s): C16.320.798.500, C20.673.795.500

MeSH Unique ID: D000081208

Entry Terms:

• Inherited Complement Deficiency Diseases
• Complement Deficiencies
• Complement Deficiency

Previous Indexing:

• Complement System Proteins (1971-2019)
• Immunologic Deficiency Syndromes (1971-2019)

All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Primary Immunodeficiency Diseases
Hereditary Complement Deficiency Diseases
Angioedemas, Hereditary

All MeSH Categories
Diseases Category
Immune System Diseases
Immunologic Deficiency Syndromes
Primary Immunodeficiency Diseases
Hereditary Complement Deficiency Diseases
Angioedemas, Hereditary