Hereditary Complement Deficiency Diseases

Go to external page http://id.nlm.nih.gov/mesh/D000081208


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).

Synonyms: Inherited Complement Deficiency Diseases, Complement Deficiencies, Complement Deficiency, Hereditary Complement Deficiency Diseases

Instance information

comment

2020

identifier

D000081208