Disease

hereditary spastic paraplegia 2

Name: hereditary spastic paraplegia 2
Creator: Alliance of Genome Resources
License: CC BY 4.0
Keywords: disease DOID:0110773 hereditary spastic paraplegia 2 A hereditary spastic paraplegia that has_material_basis_in mutation in the PLP1 gene on chromosome Xq22.2. SPG2 X-linked spastic paraplegia 2 spastic paraplegia type 2

Definition

A hereditary spastic paraplegia that has_material_basis_in mutation in the PLP1 gene on chromosome Xq22.2.

Synonyms

spastic paraplegia type 2
SPG2

Cross References

GARD:4923
ICD10CM:G11.4

Parent Terms

hereditary spastic paraplegia
X-linked recessive disease

Child Terms

None

Sources of Associations

RGD
MGI
ZFIN
FB
WB
SGD

Associated Genes

Gene	Species	Association	Disease Qualifier	Disease	Evidence	Based On	Source	References
No records match query. Try removing filters.

Showing 0 - 0 of 0 rows

per page

Associated Alleles

Allele	Species	Association	Disease Qualifier	Disease	Evidence	Source	References
No records match query. Try removing filters.

Showing 0 - 0 of 0 rows

per page

Associated Models

Model	Species	Experimental condition	Association	Disease Qualifiers	Disease	Condition Modifier	Genetic Modifier	Evidence	Source	References
No records match query. Try removing filters.

Showing 0 - 0 of 0 rows

per page