Disease

hereditary spastic paraplegia 41

Name: hereditary spastic paraplegia 41
Creator: Alliance of Genome Resources
License: CC BY 4.0
Keywords: disease DOID:0110793 hereditary spastic paraplegia 41 A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 11p14.1-p11.2. autosomal dominant spastic paraplegia 41 autosomal dominant spastic paraplegia type 41 SPG41

Definition

A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 11p14.1-p11.2.

Synonyms

autosomal dominant spastic paraplegia 41
autosomal dominant spastic paraplegia type 41

Cross References

ICD10CM:G11.4
MIM:613364

Parent Terms

autosomal dominant 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