Search Ontology:
Human Disease
hereditary spastic paraplegia 30B
- Term ID
- DOID:0070646
- Synonyms
-
- Definition
- A hereditary spastic paraplegia 30 that has_material_basis_in homozygous mutation in the KIF1A gene on chromosome 2q37. https://pubmed.ncbi.nlm.nih.gov/21487076/
- References
- Ontology
- Human Disease ( DOID:0070646 )
Other Pages
Genes Involved
Zebrafish Models