Disease #05614

Official abbreviation DYTOABG
Name dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities (DYTOABG)
OMIM ID 617282
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene MECR
Associated tissues -
Disease features autosomal recessive
Remarks -