hereditary spastic paraplegia 42

Term ID

DOID:0110794

Synonyms

autosomal dominant spastic paraplegia 42
autosomal dominant spastic paraplegia type 42
SPG42

Definition

A hereditary spastic paraplegia that has_material_basis_in mutation in the SLC33A1 gene on chromosome 3q25.31. https://www.ncbi.nlm.nih.gov/pubmed/19061983

References

ICD10CM:G11.4
MIM:612539
ORDO:171863

Ontology

Human Disease ( DOID:0110794 )

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