Disease association ontology term - MONDO:0014702 - autosomal recessive complex spastic paraplegia type 9B
Term summary
- ID
- MONDO:0014702
- Name
- autosomal recessive complex spastic paraplegia type 9B
- Ontology or CV name
- Disease association
- Definition
- Any autosomal recessive complex spastic paraplegia in which the cause of the disease is a mutation in the ALDH18A1 gene.
