Term Name: | hereditary spastic paraplegia 18B |
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Synonyms: | spastic paraplegia 18B |
Definition: | A hereditary spastic paraplegia 18 that has_material_basis_in homozygous mutation in the ERLIN2 gene on chromosome 8p11. |
Ontology: | Human Disease [DOID:0070641] ( DOID:0070641 ) |