Disease #05201

Official abbreviation SPG-76
Name paraplegia, spastic, autosomal recessive, type 76 (SPG-76)
OMIM ID 616907
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene CAPN1
Associated tissues -
Disease features -
Remarks -