MeSH Browser

MeSH Supplementary: Mannose-Binding Protein Deficiency
Unique ID: C563602
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563602
Entry Term(s): MBL Deficiency; MBL2 Deficiency; MBP Deficiency; Mannose-Binding Lectin Deficiency; Mannose-Binding Lectin Protein Deficiency
Heading Mapped to: *Metabolism, Inborn Errors; Mannose-Binding Lectin / deficiency
Frequency: 51
Note: A condition characterized by a mannose-binding lectin (MBL) protein level of less than 100 ng/ml, that occurs in about 5% of people of European descent and in about 10% of sub-Saharan Africans. Most MBL-deficient adults appear healthy, but low levels of MBL are associated with increased risk of infection in toddlers, in cancer patients undergoing chemotherapy, and in organ-transplant patients receiving immunosuppressive drugs, particularly recipients of liver transplants. Polymorphisms in the MBL2 gene have been identified. OMIM: 614372
Date of Entry: 2012/11/05
Revision Date: 2015/09/26

Concept UI: M0563902
Terms: Mannose-Binding Protein Deficiency Preferred Term
Term UI T803220
Date11/15/2011
LexicalTag NON
ThesaurusID; Mannose-Binding Lectin Deficiency
Term UI T841954
Date04/18/2013
LexicalTag NON
ThesaurusID GHR (2014); Mannose-Binding Lectin Protein Deficiency
Term UI T841955
Date04/18/2013
LexicalTag NON
ThesaurusID GHR (2014); MBL2 Deficiency
Term UI T845985
Date06/21/2013
LexicalTag NON
ThesaurusID GHR (2014); MBP Deficiency
Term UI T845986
Date06/21/2013
LexicalTag NON
ThesaurusID GHR (2014); MBL Deficiency
Term UI T845987
Date06/21/2013
LexicalTag NON
ThesaurusID GHR (2014)

Mannose-Binding Protein Deficiency MeSH Supplementary Concept Data 2024