MeSH Browser

MeSH Supplementary: Complement Factor I Deficiency
Unique ID: C572568
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C572568
Entry Term(s): C3 Inactivator Deficiency; C3G2 C3 glomerulopathy 2; Complement Component 3 Inactivator Deficiency
Previous Indexing: GENETIC DISEASES, INBORN (2014-2019)
Heading Mapped to: Complement C3 / deficiency; *Hereditary Complement Deficiency Diseases
Frequency: 12
Date of Entry: 2012/08/24
Revision Date: 2022/11/02

Complement Factor I Deficiency MeSH Supplementary Concept Data 2024