Disease

hereditary spastic paraplegia 43

Name: hereditary spastic paraplegia 43
Creator: Alliance of Genome Resources
License: CC BY 4.0
Keywords: disease DOID:0110795 hereditary spastic paraplegia 43 A hereditary spastic paraplegia that has_material_basis_in mutation in the C19ORF12 gene on chromosome 19q12. autosomal recessive spastic paraplegia 43 SPG43 autosomal recessive spastic paraplegia type 43

Definition

A hereditary spastic paraplegia that has_material_basis_in mutation in the C19ORF12 gene on chromosome 19q12.

Synonyms

autosomal recessive spastic paraplegia 43
autosomal recessive spastic paraplegia type 43

Cross References

ICD10CM:G11.4
MIM:615043

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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