isolated growth hormone deficiency type II

Summary
Synonym
  • IGHD II
  • autosomal dominant isolated growth hormone deficiency
  • autosomal dominant pituitary dwarfism due to isolated growth hormone deficiency
  • congenital IGHD type II
  • congenital isolated GH deficiency type II
  • congenital isolated growth hormone deficiency type II
Definition
An isolated growth hormone deficiency characterized by autosomal dominant inheritance of low but detectable levels of GH1 resulting in variable degrees of dwarfism which are responsive to growth hormone therapy that has_material_basis_in dominant negative mutations in the GH1 gene on chromosome 17q23.3.
Super Class
isolated growth hormone deficiency
Related Genes
Displaying entries 11 - 20 of 22 in total
Gene ID Gene Symbol Description Source
3293 HSD17B3 hydroxysteroid 17-beta dehydrogenase 3
3897 L1CAM L1 cell adhesion molecule
4594 MMUT methylmalonyl-CoA mutase
4907 NT5E 5'-nucleotidase ecto
5373 PMM2 phosphomannomutase 2
6296 ACSM3 acyl-CoA synthetase medium chain family member 3
6646 SOAT1 sterol O-acyltransferase 1
8482 SEMA7A semaphorin 7A (JohnMiltonHagen blood group)
9394 HS6ST1 heparan sulfate 6-O-sulfotransferase 1
10908 PNPLA6 patatin like phospholipase domain containing 6

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024