Disease

hereditary spastic paraplegia 18

Name: hereditary spastic paraplegia 18
Creator: Alliance of Genome Resources
License: CC BY 4.0
Keywords: disease DOID:0110771 hereditary spastic paraplegia 18 A hereditary spastic paraplegia that has_material_basis_in mutation in the ERLIN2 gene on chromosome 8p11. intellectual disability, motor dysfunction and joint contractures autosomal recessive spastic paraplegia 18 IDMDC SPG18 autosomal recessive spastic paraplegia type 18

Definition

A hereditary spastic paraplegia that has_material_basis_in mutation in the ERLIN2 gene on chromosome 8p11.

Synonyms

autosomal recessive spastic paraplegia 18
autosomal recessive spastic paraplegia type 18

Cross References

GARD:4922
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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