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Echinobase
Summary Literature (0)
DOID:0110783 - hereditary spastic paraplegia 32

Disease Ontology Definition:A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 14q12-q21.

Synonyms: SPG32, autosomal recessive spastic paraplegia 32, autosomal recessive spastic paraplegia type 32,

Echinobase Genes :



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

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