Search Ontology:
Human Disease
hereditary spastic paraplegia 18A
- Term ID
- DOID:0070640
- Synonyms
-
- autosomal dominant spastic paraplegia 18
- spastic paraplegia 18A
- Definition
- A hereditary spastic paraplegia 18 that has_material_basis_in heterozygous mutation in the ERLIN2 gene on chromosome 8p11. (2)
- References
- Ontology
- Human Disease ( DOID:0070640 )
Other Pages
Genes Involved
Zebrafish Models