hereditary spastic paraplegia 63

Term ID

DOID:0110814

Synonyms

autosomal recessive spastic paraplegia 63
spastic paraplegia 63
SPG63

Definition

A hereditary spastic paraplegia that has_material_basis_in mutation in the AMPD2 gene on chromosome 1p13. https://www.ncbi.nlm.nih.gov/pubmed/24482476

References

ICD10CM:G11.4
MIM:615686
ORDO:401805

Ontology

Human Disease ( DOID:0110814 )

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