hereditary spastic paraplegia 64

Term ID

DOID:0110815

Synonyms

autosomal recessive spastic paraplegia 64
autosomal recessive spastic paraplegia type 64
SPG64

Definition

A hereditary spastic paraplegia that has_material_basis_in mutation in the ENTPD1 gene on chromosome 10q24. https://www.ncbi.nlm.nih.gov/pubmed/24482476

References

ICD10CM:G11.4
MIM:615683
ORDO:401810

Ontology

Human Disease ( DOID:0110815 )

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