MeSH Browser

MeSH Supplementary: Complement Component 6 Deficiency
Unique ID: C567307
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567307
Entry Term(s): C6 Deficiency
Registry Numbers: 0
Previous Indexing: IMMUNOLOGIC DEFICIENCY SYNDROMES (2014-2019)
Heading Mapped to: Complement C6 / deficiency; *Hereditary Complement Deficiency Diseases
Frequency: 9
Note: mutation in C6 gene
Date of Entry: 2012/11/05
Revision Date: 2019/06/17

Complement Component 6 Deficiency MeSH Supplementary Concept Data 2025