hereditary spastic paraplegia 63

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Echinobase

Summary

Literature (0)

DOID:0110814 - hereditary spastic paraplegia 63

Disease Ontology Definition:A hereditary spastic paraplegia that has_material_basis_in mutation in the AMPD2 gene on chromosome 1p13.

Synonyms: autosomal recessive spastic paraplegia 63, spastic paraplegia 63, SPG63

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

: ampd2

MIM:

MIM:615686 - spastic paraplegia 63, autosomal recessive; spg63

MIM:615686 - spastic paraplegia 63, autosomal recessive; spg63

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)