Disease

hereditary spastic paraplegia 48

Name: hereditary spastic paraplegia 48
Creator: Alliance of Genome Resources
License: CC BY 4.0
Keywords: disease DOID:0110800 hereditary spastic paraplegia 48 A hereditary spastic paraplegia that has_material_basis_in mutation in the AP5Z1 gene on chromosome 7p22.1. autosomal recessive spastic paraplegia type 48 SPG48 autosomal recessive spastic paraplegia 48

Definition

A hereditary spastic paraplegia that has_material_basis_in mutation in the AP5Z1 gene on chromosome 7p22.1.

Synonyms

autosomal recessive spastic paraplegia 48
autosomal recessive spastic paraplegia type 48

Cross References

ICD10CM:G11.4
MIM:613647

Parent Terms

autosomal recessive disease
hereditary spastic paraplegia

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