hereditary spastic paraplegia 29

Term ID

DOID:0110780

Synonyms

autosomal dominant spastic paraplegia 29
SPG29

Definition

A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 1p31.1-p21.1. https://www.ncbi.nlm.nih.gov/pubmed/16130112

References

GARD:9729
ICD10CM:G11.4
MIM:609727
ORDO:101009

Ontology

Human Disease ( DOID:0110780 )

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

Citations