Disease #06012 (SPG78 (Spastic paraplegia 78, autosomal recessive), OMIM:617225)

Official abbreviation SPG78
Name Spastic paraplegia 78, autosomal recessive
OMIM ID 617225
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene ATP13A2
Associated tissues -
Disease features -
Remarks -