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

47 clinical trials for this condition and its sub-types, 0 tagged with Aceruloplasminemia itself.

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↑ Inherited retinal dystrophy (513) ↑ Hereditary anemia (13) ↑ Disorder of iron metabolism and transport (9) ↑ Neurodegeneration with brain iron accumulation (8)

Including sub-types (47) Tagged with Aceruloplasminemia (0)

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