All conditions under G

Conditions

• Galactokinase deficiency with cataracts

  Associated gene: GALK1

• Galactosaemia

  Associated gene: GALT

• Gastrointestinal defects and immunodeficiency syndrome

  Associated gene: TTC7A

• Generalised arterial calcification of infancy
  2 associated genes

  • ENPP1
  • ABCC6
• Glanzmann thrombasthenia
  2 associated genes

  • ITGA2B
  • ITGB3
• Glucocorticoid deficiency
  3 associated genes

  • MC2R
  • MRAP
  • NNT
• Glucose/galactose malabsorption

  Associated gene: SLC5A1

• GLUT1 deficiency syndrome

  Associated gene: SLC2A1

• Glutaric aciduria type I

  Associated gene: GCDH

• Glycogen storage disease II (Pompe Disease)

  Associated gene: GAA

• Glycogen storage disease type I
  2 associated genes

  • G6PC1
  • SLC37A4
• Glycogen storage disease type III

  Associated gene: AGL

• Griscelli Syndrome

  Associated gene: RAB27A

• Growth hormone receptor deficiency

  Associated gene: GHR

• Growth hormone-secreting pituitary adenoma-2

  Associated gene: GPR101