MeSH Browser

MeSH Supplementary: Properdin deficiency, X-linked
Unique ID: C537241
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537241
Entry Term(s): Properdin Deficiency, Type I; Properdin P factor deficiency; Properdin deficiency, type 1
Registry Number: 0
Heading Mapped to: *Hereditary Complement Deficiency Diseases; Properdin / *deficiency; *Genetic Diseases, X-Linked
Frequency: 0
Date of Entry: 2010/08/25
Revision Date: 2019/06/17

Properdin deficiency, X-linked MeSH Supplementary Concept Data 2024