Disease

hereditary spastic paraplegia 39

Name: hereditary spastic paraplegia 39
Creator: Alliance of Genome Resources
License: CC BY 4.0
Keywords: disease DOID:0110790 hereditary spastic paraplegia 39 A hereditary spastic paraplegia that has_material_basis_in mutation in the PNPLA6 gene on chromosome 19p13. NTE-related motor neuron disorder autosomal recessive spastic paraplegia 39 NTEMND spastic paraplegia due to NTE mutation SPG39 autosomal recessive spastic paraplegia type 39 spastic paraplegia due to neuropathy target esterase mutation

Definition

A hereditary spastic paraplegia that has_material_basis_in mutation in the PNPLA6 gene on chromosome 19p13.

Synonyms

autosomal recessive spastic paraplegia 39
autosomal recessive spastic paraplegia type 39

Cross References

GARD:4924
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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