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Hypogammaglobulinemia and Isolated growth hormone deficiency, X-linked MeSH Supplementary Concept Data 2022


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 Number
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 Preferred
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