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Summary Literature (0)
DOID:0110738 - neurodegeneration with brain iron accumulation 4

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

Synonyms: Mitochondrial Protein-Associated Neurodegeneration, MPAN, NBIA4, NBIA due to C19orf12 mutation, Neurodegeneration with brain iron accumulation due to C19orf12 mutation, Neurodegeneration with brain iron accumulation type 4

Xenbase Genes : c4h19orf12

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013674 - neurodegeneration with brain iron accumulation 4


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive disease (is_a), neurodegeneration with brain iron accumulation (is_a)