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Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Primary Immunodeficiency Diseases > Hereditary Complement Deficiency Diseases
Immune System Diseases > Immunologic Deficiency Syndromes > Primary Immunodeficiency Diseases > Hereditary Complement Deficiency Diseases

Preferred term

Hereditary Complement Deficiency Diseases  

Type

  • Topical Descriptor

Broader concept

Narrower concepts

Entry terms

  • Inherited Complement Deficiency Diseases

Scope note

  • 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

  • 2020

In other languages

URI

http://www.yso.fi/onto/mesh/D000081208

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