MeSH Browser

MeSH Supplementary: Complement Component 4a Deficiency
Unique ID: C565167
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565167
Registry Numbers: 0
Previous Indexing: IMMUNOLOGIC DEFICIENCY SYNDROMES (2014-2019)
Heading Mapped to: Complement C4a / deficiency; *Hereditary Complement Deficiency Diseases
Frequency: 3
Note: mutation in C4A
Date of Entry: 2012/11/05
Revision Date: 2019/06/17

Complement Component 4a Deficiency MeSH Supplementary Concept Data 2025