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 MIM:609727 ORDO:101009
Subsets	DO_rare_slim
Synonyms	autosomal dominant spastic paraplegia 29 [EXACT] SPG29 [EXACT]
Parent Relationships	is_a hereditary spastic paraplegia is_a autosomal dominant disease