MeSH Browser

MeSH Supplementary: Complement Factor D Deficiency
Unique ID: C565027
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565027
Entry Term(s): Factor D Deficiency
Registry Number: 0
Previous Indexing: IMMUNOLOGIC DEFICIENCY SYNDROMES (2014-2019)
Heading Mapped to: *Hereditary Complement Deficiency Diseases; Complement Factor D / *deficiency; *Glomerulonephritis, Membranoproliferative
Frequency: 3
Note: mutation in CFD
Date of Entry: 2012/11/05
Revision Date: 2022/11/02

Complement Factor D Deficiency MeSH Supplementary Concept Data 2024