Disease

hereditary spastic paraplegia 46

Name: hereditary spastic paraplegia 46
Creator: Alliance of Genome Resources
License: CC BY 4.0
Keywords: disease DOID:0110798 hereditary spastic paraplegia 46 A hereditary spastic paraplegia that has_material_basis_in mutation in the GBA2 gene on chromosome 9p. SPG46 autosomal recessive spastic paraplegia 46 autosomal recessive spastic paraplegia type 46

Definition

A hereditary spastic paraplegia that has_material_basis_in mutation in the GBA2 gene on chromosome 9p.

Synonyms

autosomal recessive spastic paraplegia 46
autosomal recessive spastic paraplegia type 46

Cross References

ICD10CM:G11.4
MIM:614409

Parent Terms

autosomal recessive disease
hereditary spastic paraplegia

Child Terms

None

Sources of Associations

RGD
MGI
ZFIN
FB
WB
SGD

Associated Genes

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Associated Alleles

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Associated Models

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