hereditary spastic paraplegia 37

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Summary

Literature (0)

DOID:0110788 - hereditary spastic paraplegia 37

Disease Ontology Definition:A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 8p21.1-q13.3.

Synonyms: SPG37, autosomal dominant spastic paraplegia 37, autosomal dominant spastic paraplegia type 37,

Echinobase 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

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

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

Parent(s): autosomal dominant disease (is_a), hereditary spastic paraplegia (is_a)