Disease

hereditary spastic paraplegia 19

Name: hereditary spastic paraplegia 19
Creator: Alliance of Genome Resources
License: CC BY 4.0
Keywords: disease DOID:0110772 hereditary spastic paraplegia 19 A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 9q. autosomal dominant spastic paraplegia 19 SPG19 autosomal dominant spastic paraplegia type 19

Definition

A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 9q.

Synonyms

autosomal dominant spastic paraplegia 19
autosomal dominant spastic paraplegia type 19

Cross References

GARD:9588
ICD10CM:G11.4

Parent Terms

autosomal dominant 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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