Search Ontology: 
        
        Human Disease
            hereditary spastic paraplegia 7
- Term ID
 - DOID:0110816
 - Synonyms
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- autosomal recessive spastic paraplegia 7
 - spastic paraplegia type 7
 - SPG7
 
 - Definition
 - A hereditary spastic paraplegia that is characterized by slowly progressive onset, usually between 18-60 years of age, and generally more severe spasticity and has_material_basis_in mutation in the SPG7 gene on chromosome 16q24. https://www.ncbi.nlm.nih.gov/pubmed/9635427
 - References
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- ICD10CM:G11.4
 - MIM:607259
 - ORDO:99013
 
 - Ontology
 - Human Disease ( DOID:0110816 )
 
                
                    
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                        Zebrafish Models