hereditary spastic paraplegia 31

Term ID

DOID:0110782

Synonyms

autosomal dominant spastic paraplegia 31
autosomal dominant spastic paraplegia type 31
SPG31

Definition

A hereditary spastic paraplegia that has_material_basis_in mutation in the REEP1 gene on chromosome 2p11. https://www.ncbi.nlm.nih.gov/pubmed/16826527

References

GARD:10817
ICD10CM:G11.4
MIM:610250
ORDO:101011

Ontology

Human Disease ( DOID:0110782 )

Relationships

is a type of: autosomal dominant disease hereditary spastic paraplegia

autosomal dominant disease hereditary spastic paraplegia Show first 5 Terms

Other Pages

Alliance (1)

Genes Involved

Zebrafish Models