hereditary spastic paraplegia 76

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Summary

Literature (0)

DOID:0110821 - hereditary spastic paraplegia 76

Disease Ontology Definition:A hereditary spastic paraplegia that has_material_basis_in mutation in the CAPN1 gene on chromosome 11q13.

Synonyms: SPG76, autosomal recessive spastic paraplegia 76,

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

: capn1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014827 - autosomal recessive spastic paraplegia type 76

MONDO:0014827 - autosomal recessive spastic paraplegia type 76

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)