MeSH Browser

MeSH Supplementary: Say Barber Miller syndrome
Unique ID: C536618
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536618
Entry Term(s): Microcephaly hypogammaglobulinemia abnormal immunity
Registry Numbers: 0
Heading Mapped to: Agammaglobulinemia / congenital; *Microcephaly
Frequency: 0
Note: Microcephaly with chemotactic defect and transient hypogammaglobulinemia
Date of Entry: 2010/08/25
Revision Date: 2013/11/06

Say Barber Miller syndrome MeSH Supplementary Concept Data 2025