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Metadata
ID DOID:0110766
Name hereditary spastic paraplegia 13
Definition A hereditary spastic paraplegia that is characterized by a pure form of the disease with late onset and has_material_basis_in mutation in the HSPD1 gene on chromosome 2q33.
https://www.ncbi.nlm.nih.gov/pubmed/11898127
Xrefs

GARD:9616

ICD10CM:G11.4

OMIM:605280

ORDO:100994

Subsets

DO_rare_slim

Synonyms

autosomal dominant spastic paraplegia 13 [EXACT]

SPG13 [EXACT]

Parent Relationships

is_a hereditary spastic paraplegia

is_a autosomal dominant disease

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