MeSH Browser

MeSH Supplementary: MASP2 Deficiency
Unique ID: C565360
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565360
Registry Number: 0
Previous Indexing: IMMUNOLOGIC DEFICIENCY SYNDROMES (2013-2019)
Heading Mapped to: *Hereditary Complement Deficiency Diseases; Mannose-Binding Protein-Associated Serine Proteases / *deficiency
Frequency: 1
Note: mutation in MASP2
Date of Entry: 2012/11/05
Revision Date: 2019/06/17

MASP2 Deficiency MeSH Supplementary Concept Data 2023