Search Ontology: 
        
        Human Disease
            hereditary spastic paraplegia 91
- Term ID
 - DOID:0070643
 - Synonyms
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- autosomal dominant spastic paraplegia 91
 - autosomal dominant spastic paraplegia 91 with or without cerebellar ataxia
 
 - Definition
 - A hereditary spastic paraplegia that has_material_basis_in heterozygous mutation in the SPTAN1 gene on chromosome 9q34. (2)
 - References
 - Ontology
 - Human Disease ( DOID:0070643 )
 
                
                    
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                        Zebrafish Models