Visualize Submit Comment
Metadata
ID DOID:0110780
Name hereditary spastic paraplegia 29
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
Xrefs

GARD:9729

ICD10CM:G11.4

OMIM:609727

ORDO:101009

Synonyms

autosomal dominant spastic paraplegia 29 [EXACT]

SPG29 [EXACT]

Parent Relationships

is_a hereditary spastic paraplegia

Add an item to the term tracker