Phenotypes for disease #02300 (SPG6 (paraplegia, spastic, type 6 (SPG-6)), OMIM:600363)

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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000041539 pure hereditary spastic paraplegia hereditary spastic paraplegia SPG8 Familial, autosomal dominant - - 53y - - Erik-Jan Kamsteeg 00054874
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