Term Name:	isolated growth hormone deficiency type III
Synonyms:	congenital IGHD type III, congenital isolated GH deficiency type III, congenital isolated growth hormone deficiency type III, Fleisher syndrome, growth hormone deficiency with hypogammaglobulinemia, IGHD III, X-linked agammaglobulinemia and isolated growth hormone deficiency, X-linked hypogammaglobulinemia and isolated growth hormone deficiency, X-linked IGHD, X-linked isolated growth hormone deficiency
Definition:	An isolated growth hormone deficiency characterized by dwarfism, variable occurence of hypogammaglobulinemia, and a generally good response to growth hormone therapy that has_material_basis_in mutation in the BTK gene on chromosome Xq22.1.
Ontology:	Human Disease [DOID:0060875]   ( DOID:0060875 )