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Metadata
ID DOID:0110765
Name hereditary spastic paraplegia 12
Definition A hereditary spastic paraplegia that has_material_basis_in mutation in the RTN2 gene on chromosome 19q13.
https://www.ncbi.nlm.nih.gov/pubmed/22232211
Xrefs

GARD:9586

ICD10CM:G11.4

MIM:604805

ORDO:100993

Subsets

DO_rare_slim

Synonyms

autosomal dominant spastic paraplegia 12 [EXACT]

autosomal dominant spastic paraplegia type 12 [EXACT]

SPG12 [EXACT]

Parent Relationships

is_a hereditary spastic paraplegia

is_a autosomal dominant disease

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