Disease #03663 (SPAX-5 (ataxia, spastic, type 5, autosomal recessive (SPAX-5)), OMIM:614487)

Official abbreviation SPAX-5
Name ataxia, spastic, type 5, autosomal recessive (SPAX-5)
OMIM ID 614487
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene AFG3L2
Associated tissues -
Disease features -
Remarks -