| Metadata | |
|---|---|
| ID | DOID:0110786 |
| Name | hereditary spastic paraplegia 35 |
| Definition | A hereditary spastic paraplegia that has_material_basis_in mutation in the FA2H gene on chromosome 16q23.1. https://www.ncbi.nlm.nih.gov/pubmed/19068277 |
| Xrefs | |
| Subsets |
DO_rare_slim |
| Synonyms |
autosomal recessive spastic paraplegia 35 [EXACT] autosomal recessive spastic paraplegia type 35 [EXACT] FAHN [EXACT] fatty acid hydroxylase-associated neurodegeneration [EXACT] leukodystrophy, dysmyelinating and spastic paraparesis with or without dystonia [EXACT] SPG35 [EXACT] |
| Parent Relationships |