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DOID:0110737 - neurodegeneration with brain iron accumulation 3
Disease Ontology Definition:A neurodegeneration with brain iron accumulation that has_material_basis_in autosomal dominant inheritance of mutation in the FTL gene on chromosome 19q13.33.
Synonyms: Adult basal ganglia disease, Ferritin-related neurodegeneration, Hereditary ferritinopathy, NBIA3, Neuroferritinopathy, Neuroferritinopathy; Basal Ganglia Disease, Adult-Onset,
Xenbase Genes :
MONDO:0011638 - neuroferritinopathy |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee