hereditary spastic paraplegia 12

Term ID

DOID:0110765

Synonyms

autosomal dominant spastic paraplegia 12
autosomal dominant spastic paraplegia type 12
SPG12

Definition

A hereditary spastic paraplegia that has_material_basis_in mutation in the RTN2 gene on chromosome 19q13. https://www.ncbi.nlm.nih.gov/pubmed/22232211

References

GARD:9586
ICD10CM:G11.4
MIM:604805
ORDO:100993

Ontology

Human Disease ( DOID:0110765 )

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