hereditary spastic paraplegia 32

Summary

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

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

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Mondo Disease Ontology (on Monarch Initiative):

MONDO:0012643 - hereditary spastic paraplegia 32

MONDO:0012643 - hereditary spastic paraplegia 32

MIM:

MIM:611252 - SPASTIC PARAPLEGIA 32, AUTOSOMAL RECESSIVE; SPG32

MIM:611252 - SPASTIC PARAPLEGIA 32, AUTOSOMAL RECESSIVE; SPG32

Other Model Organisms: Alliance, 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)