Disease #04430 (SPG-73 (paraplegia, spastic?, autosomal dominant, type 73 (SPG-73)), OMIM:616282)

Official abbreviation SPG-73
Name paraplegia, spastic?, autosomal dominant, type 73 (SPG-73)
OMIM ID 616282
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene CPT1C
Associated tissues -
Disease features -
Remarks -