hereditary spastic paraplegia 45

Term ID

DOID:0110797

Synonyms

autosomal recessive spastic paraplegia 45
autosomal recessive spastic paraplegia type 45
autosomal recessive spastic paraplegia type 65
SPG45
SPG65

Definition

A hereditary spastic paraplegia that has_material_basis_in mutation in the NT5C2 gene on chromosome 10q24. https://www.ncbi.nlm.nih.gov/pubmed/24482476

References

ICD10CM:G11.4
MIM:613162
ORDO:320396

Ontology

Human Disease ( DOID:0110797 )

Relationships

is a type of: autosomal recessive disease hereditary spastic paraplegia

autosomal recessive disease hereditary spastic paraplegia Show first 5 Terms

Other Pages

Alliance (1)

Genes Involved

Zebrafish Models