Disease

hereditary spastic paraplegia 37

Name: hereditary spastic paraplegia 37
Creator: Alliance of Genome Resources
License: CC BY 4.0
Keywords: disease DOID:0110788 hereditary spastic paraplegia 37 A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 8p21.1-q13.3. SPG37 autosomal dominant spastic paraplegia type 37 autosomal dominant spastic paraplegia 37

Definition

A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 8p21.1-q13.3.

Synonyms

autosomal dominant spastic paraplegia 37
autosomal dominant spastic paraplegia type 37

Cross References

ICD10CM:G11.4
MIM:611945

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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