Metadata | |
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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 | |
Subsets |
DO_rare_slim |
Synonyms |
autosomal dominant spastic paraplegia 12 [EXACT] autosomal dominant spastic paraplegia type 12 [EXACT] SPG12 [EXACT] |
Parent Relationships |