MeSH Browser

MeSH Supplementary: Hypogammaglobulinemia and Isolated growth hormone deficiency, X-linked
Unique ID: C537149
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537149
Entry Term(s): Agammaglobulinemia and isolated growth hormone deficiency, X-linked; Fleisher syndrome; Growth Hormone Deficiency with Hypogammaglobulinemia; Isolated Growth Hormone Deficiency, Type III; Isolated growth hormone deficiency, type 3; Nanism due to growth hormone isolated deficiency with X-linked hypogammaglobulinemia
Registry Numbers: 0
Heading Mapped to: *Agammaglobulinemia; *Dwarfism, Pituitary; *Genetic Diseases, X-Linked
Frequency: 0
Date of Entry: 2010/08/25
Revision Date: 2012/08/24

Hypogammaglobulinemia and Isolated growth hormone deficiency, X-linked MeSH Supplementary Concept Data 2025