aceruloplasminemia Gene Set

Dataset DISEASES Curated Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description An iron metabolism disease that has_material_basis_in a mutation in the ceruloplasmin gene characterized by progressive neurodegeneration of the retina and basal ganglia and diabetes mellitus. (Human Disease Ontology, DOID_0050711)
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Genes

1 genes involed in the disease aceruloplasminemia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
CP ceruloplasmin (ferroxidase)