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Echinobase
Summary Literature (0)
DOID:0110821 - hereditary spastic paraplegia 76

Disease Ontology Definition:A hereditary spastic paraplegia that has_material_basis_in mutation in the CAPN1 gene on chromosome 11q13.

Synonyms: SPG76, autosomal recessive spastic paraplegia 76,

Echinobase Genes :



Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): hereditary spastic paraplegia (is_a)