A neurodegeneration with brain iron accumulation that has_material_basis_in autosomal recessive inheritance of mutation in the C19orf12 gene on chromosome 19q12.
synonyms:
ORDO:289560,
ICD10CM:G23.0,
NBIA4,
NBIA due to C19orf12 mutation,
Neurodegeneration with brain iron accumulation type 4,
MPAN,
OMIM:614298,
614298,
Neurodegeneration with brain iron accumulation due to C19orf12 mutation,