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Metadata
ID DOID:0110763
Name hereditary spastic paraplegia 10
Definition A hereditary spastic paraplegia that has_material_basis_in mutation in the KIF5A gene on chromosome 12q13.
https://www.ncbi.nlm.nih.gov/pubmed/12355402
Xrefs

GARD:9590

ICD10CM:G11.4

OMIM:604187

ORDO:100991

Subsets

DO_rare_slim

Synonyms

autosomal dominant spastic paraplegia 10 [EXACT]

autosomal dominant spastic paraplegia type 10 [EXACT]

SPG10 [EXACT]

Parent Relationships

is_a hereditary spastic paraplegia

is_a autosomal dominant disease

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