Metadata | |
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ID | DOID:0110818 |
Name | hereditary spastic paraplegia 73 |
Definition | A hereditary spastic paraplegia that has_material_basis_in mutation in the CPT1C gene on chromosome 19q13. https://www.ncbi.nlm.nih.gov/pubmed/25751282 |
Xrefs | |
Subsets |
DO_rare_slim |
Synonyms |
autosomal dominant spastic paraplegia 73 [EXACT] autosomal dominant spastic paraplegia type 73 [EXACT] SPG73 [EXACT] |
Parent Relationships |