Disorder Of Copper Metabolism
An inherited metabolic disease that is has its basis in the disruption of cellular copper ion homeostasis.
Známé také jako
copper Transport disorders; inborn cellular copper ion homeostasis disorder; inborn error of cellular copper ion homeostasis; rare inborn error of cellular copper ion homeostasis
Zahrnuje 6 příbuzných podtypů ↓Skrýt podtypy ↑
- autosomal recessive axonal charcot-marie-tooth disease due to copper metabolism defect
- familial benign copper deficiency
- MEDNIK syndrome
- Menkes disease
- occipital horn syndrome
- Wilson disease
