Disease #01297 (DYT12 (dystonia, type 12 (DYT-12)), OMIM:128235)

Official abbreviation DYT12
Name dystonia, type 12 (DYT-12)
OMIM ID 128235
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene ATP1A3
Associated tissues -
Disease features -
Remarks -