Summary Literature (0)

DOID:0110794 - hereditary spastic paraplegia 42

Disease Ontology Definition:A hereditary spastic paraplegia that has_material_basis_in mutation in the SLC33A1 gene on chromosome 3q25.31.

Synonyms: autosomal dominant spastic paraplegia 42, autosomal dominant spastic paraplegia type 42, SPG42

Xenbase Genes : slc33a1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0012928 - hereditary spastic paraplegia 42

MIM:

MIM:612539 - SPASTIC PARAPLEGIA 42, AUTOSOMAL DOMINANT; SPG42

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee