Aceruloplasminemia
From Wikipedia, the free encyclopedia
| ICD-10 | E83.0 |
|---|---|
| ICD-9 | 275.0 |
Aceruloplasminemia is an autosomal recessive disorder characterized by progressive neurodegeneration of the retina and basal ganglia and diabetes mellitus. Iron accumulates in the pancreas, liver and brain. It is caused by mutations in the ceruloplasmin gene.
[edit] See also
[edit] External links
- Aceruloplasminemia - Geneva Foundation for Medical Education and Research
- Mendelian Inheritance in Man (OMIM) 604290
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