hereditary spastic paraplegia 56

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Summary

Literature (0)

DOID:0110808 - hereditary spastic paraplegia 56

Disease Ontology Definition:A hereditary spastic paraplegia that has_material_basis_in mutation in the CYP2U1 gene on chromosome 4q25.

Synonyms: SPG56, autosomal recessive spastic paraplegia 56, autosomal recessive spastic paraplegia type 56,

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

: LOC581885

OMIM:

MIM:615030 - spastic paraplegia 56, autosomal recessive; spg56

MIM:615030 - spastic paraplegia 56, autosomal recessive; spg56

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

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

Parent(s): hereditary spastic paraplegia (is_a)