isolated growth hormone deficiency type III

Summary
Synonym
  • Fleisher syndrome
  • IGHD III
  • X-linked IGHD
  • X-linked agammaglobulinemia and isolated growth hormone deficiency
  • X-linked hypogammaglobulinemia and isolated growth hormone deficiency
  • X-linked isolated growth hormone deficiency
  • congenital IGHD type III
  • congenital isolated GH deficiency type III
  • congenital isolated growth hormone deficiency type III
  • growth hormone deficiency with hypogammaglobulinemia
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.
Super Class
X-linked recessive disease isolated growth hormone deficiency
Related Genes
Displaying entries 1 - 10 of 22 in total
Gene ID Gene Symbol Description Source
128 ADH5 alcohol dehydrogenase 5 (class III), chi polypeptide
412 STS steroid sulfatase
960 CD44 CD44 molecule (IN blood group)
1586 CYP17A1 cytochrome P450 family 17 subfamily A member 1
1588 CYP19A1 cytochrome P450 family 19 subfamily A member 1
1604 CD55 CD55 molecule (Cromer blood group)
1890 TYMP thymidine phosphorylase
2619 GAS1 growth arrest specific 1
2710 GK glycerol kinase
2817 GPC1 glypican 1

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Acknowledgements

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Last updated: August 19, 2024