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 )
Relationships
Other Pages
Genes Involved
Zebrafish Models