Disease

hereditary spastic paraplegia 32

Name: hereditary spastic paraplegia 32
Creator: Alliance of Genome Resources
License: CC BY 4.0
Keywords: disease DOID:0110783 hereditary spastic paraplegia 32 A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 14q12-q21. SPG32 autosomal recessive spastic paraplegia 32 autosomal recessive spastic paraplegia type 32

Definition

A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 14q12-q21.

Synonyms

autosomal recessive spastic paraplegia 32
autosomal recessive spastic paraplegia type 32

Cross References

GARD:12749
ICD10CM:G11.4

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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