Aceruloplasminemia

MONDO:0011426

An adult-onset disorder of neurodegeneration with brain iron accumulation (NBIA) characterized by anemia, retinal degeneration, diabetes and various neurological symptoms.

Also known as: cerebellar ataxia, aceruloplasminemia, hereditary ceruloplasmin deficiency, hypoceruloplasminemia, hereditary, ceruloplasmin deficiency, familial apoceruloplasmin deficiency, hemosiderosis, systemic, due to aceruloplasminemia, hypoceruloplasminemia

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