MeSH Browser

MeSH Supplementary: MYD88 Deficiency
Unique ID: C567379
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567379
Entry Term(s): MYD88D; Pyogenic Bacterial Infections, Recurrent, Due To MYD88 Deficiency; Recurrent Pyogenic Bacterial Infections Due To MYD88 Deficiency
Registry Numbers: 0
Previous Indexing: IMMUNOLOGIC DEFICIENCY SYNDROMES (2013-2019)
Heading Mapped to: *Primary Immunodeficiency Diseases
Frequency: 26
Note: A hereditary autosomal recessive disorder caused by mutations in the MYD88 gene that result in susceptibility to severe, life-threatening, recurrent pyogenic BACTERIAL INFECTIONS in affected children, including invasive pneumococcal disease. OMIM: 612260
Date of Entry: 2012/11/05
Revision Date: 2019/06/17

MYD88 Deficiency MeSH Supplementary Concept Data 2025