Hemochromatosis type 5- MedGen UID:
- 341982
- •Concept ID:
- C1851316
- •
- Disease or Syndrome
A rare disorder of iron metabolism and transport characterised by elevated serum ferritin levels, increased serum iron, increased transferrin saturation and heavy iron deposition in hepatocytes. Iron deposition has also been indicated in heart and bone marrow, while haematological examination of peripheral blood shows no abnormalities.
Neurodegeneration and seizures due to copper transport defect- MedGen UID:
- 1841021
- •Concept ID:
- C5830385
- •
- Disease or Syndrome
Neurodegeneration and seizures due to copper transport defect (NSCT) is an autosomal recessive disorder of copper transport characterized by hypotonia, global developmental delay, seizures, and rapid brain atrophy (summary by Dame et al., 2023).