hemosiderosis

An iron metabolism disease that has_material_basis_in an accumulation of hemosiderin, an iron-storage complex, resulting in iron overload.

siderosis

A pneumoconiosis that is characterized by the deposition of excess iron in body tissue resulting from inhalation of iron in the mining dust or welding fumes.

African iron overload

A hemochromatosis characterized by a predisposition to iron loading that is exacerbated by excessive intake of dietary iron, commonly related to consumption of tradition beer brewed in non-galvanized steel drums.

hyperferritinemia-cataract syndrome

A syndrome characterized by elevated circulating levels of ferritin without iron overload and early onset cataracts that has_material_basis_in heterozygous mutation in the iron responsive element in the 5-prime noncoding region of FTL on 19q13.33.

hemochromatosis

A metal metabolism disorder characterized by the accumulation of iron in various organs of the body.

siderosis of eye

An eye degenerative disease that is characterized by intraocular iron toxicity typically due to a retained foreign body.

D-mannitol allergy

A drug allergy that has_allergic_trigger D-mannitol.

neurodegeneration with brain iron accumulation 4

A neurodegeneration with brain iron accumulation that has_material_basis_in autosomal recessive inheritance of mutation in the C19orf12 gene on chromosome 19q12.

neurodegeneration with brain iron accumulation 3

A neurodegeneration with brain iron accumulation that has_material_basis_in autosomal dominant inheritance of mutation in the FTL gene on chromosome 19q13.33.

neurodegeneration with brain iron accumulation 6

A neurodegeneration with brain iron accumulation that has_material_basis_in autosomal recessive inheritance of mutation in the COASY gene on chromosome 17q21.2.