Search Ontology:
Human Disease
hereditary spastic paraplegia 18B
- Term ID
- DOID:0070641
- Synonyms
-
- spastic paraplegia 18B
- Definition
- A hereditary spastic paraplegia 18 that has_material_basis_in homozygous mutation in the ERLIN2 gene on chromosome 8p11. (2)
- References
- Ontology
- Human Disease ( DOID:0070641 )
Other Pages
Genes Involved
Zebrafish Models