OBO ID: DOID:0050711
Term Name: aceruloplasminemia Search Ontology:
Synonyms:
Definition: 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. (2)
References:
Ontology: Human Disease   (DOID:0050711)
OTHER aceruloplasminemia PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CP Cerebellar ataxia 604290
[Hypoceruloplasminemia, hereditary] 604290
Hemosiderosis, systemic, due to aceruloplasminemia 604290
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None