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 Deficiency, Complement Deficiencies, Hereditary Complement Deficiency Diseases
Instance information
comment
2020
identifier
D000081208