MeSH Browser

MeSH Supplementary: Complement Component 3 Deficiency, Autosomal Recessive
Unique ID: C565169
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565169
Entry Term(s): C3 Deficiency, Autosomal Recessive
Previous Indexing: IMMUNOLOGIC DEFICIENCY SYNDROMES (2014-2019)
Heading Mapped to: Complement C3 / deficiency; *Hereditary Complement Deficiency Diseases
Frequency: 4
Date of Entry: 2012/11/05
Revision Date: 2019/06/17

Complement Component 3 Deficiency, Autosomal Recessive MeSH Supplementary Concept Data 2024