MeSH Browser

MeSH Supplementary: Complement Component 7 Deficiency
Unique ID: C566443
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C566443
Entry Term(s): C7 Deficiency
Previous Indexing: IMMUNOLOGIC DEFICIENCY SYNDROMES (2014-2019)
Heading Mapped to: Complement C7 / deficiency; *Hereditary Complement Deficiency Diseases
Frequency: 2
Note: mutation in C7 gene
Date of Entry: 2012/11/05
Revision Date: 2019/06/17

Complement Component 7 Deficiency MeSH Supplementary Concept Data 2024