MeSH Browser

MeSH Supplementary: Properdin Deficiency, Type II
Unique ID: C564075
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564075
Registry Numbers: 0
Previous Indexing: IMMUNOLOGIC DEFICIENCY SYNDROMES (2013-2019)
Heading Mapped to: Properdin / deficiency; *Genetic Diseases, X-Linked; *Hereditary Complement Deficiency Diseases
Frequency: 1
Date of Entry: 2012/11/05
Revision Date: 2019/06/17

Properdin Deficiency, Type II MeSH Supplementary Concept Data 2025