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hereditary spastic paraplegia 9B
Summary
- Synonym
-
- SPG9B
- autosomal recessive complex spastic paraplegia type 9B
- autosomal recessive spastic paraplegia 9B
- Definition
- A hereditary spastic paraplegia that has_material_basis_in autosomal recessive homozygous or compound heterozygous mutation in the ALDH18A1 gene on chromosome 10q24.
- Super Class
- autosomal recessive disease hereditary spastic paraplegia
External Links
- Disease Ontology
- DOID:0110825
- Mondo Disease Ontology
- ORDO
- OMIM
